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Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.
Rodan, Lance H; Spillmann, Rebecca C; Kurata, Harley T; Lamothe, Shawn M; Maghera, Jasmine; Jamra, Rami Abou; Alkelai, Anna; Antonarakis, Stylianos E; Atallah, Isis; Bar-Yosef, Omer; Bilan, Frédéric; Bjorgo, Kathrine; Blanc, Xavier; Van Bogaert, Patrick; Bolkier, Yoav; Burrage, Lindsay C; Christ, Björn U; Granadillo, Jorge L; Dickson, Patricia; Donald, Kirsten A; Dubourg, Christèle; Eliyahu, Aviva; Emrick, Lisa; Engleman, Kendra; Gonfiantini, Michaela Veronika; Good, Jean-Marc; Kalser, Judith; Kloeckner, Chiara; Lachmeijer, Guus; Macchiaiolo, Marina; Nicita, Francesco; Odent, Sylvie; O'Heir, Emily; Ortiz-Gonzalez, Xilma; Pacio-Miguez, Marta; Palomares-Bralo, María; Pena, Loren; Platzer, Konrad; Quinodoz, Mathieu; Ranza, Emmanuelle; Rosenfeld, Jill A; Roulet-Perez, Eliane; Santani, Avni; Santos-Simarro, Fernando; Pode-Shakked, Ben; Skraban, Cara; Slaugh, Rachel; Superti-Furga, Andrea; Thiffault, Isabelle; van Jaabrsveld, Richard H.
Afiliación
  • Rodan LH; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Spillmann RC; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
  • Kurata HT; Division of Medical Genetics, Department of Pediatrics, Duke Health, Durham, NC, USA.
  • Lamothe SM; Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.
  • Maghera J; Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.
  • Jamra RA; Department of Pharmacology, Alberta Diabetes Institute, University of Alberta, Edmonton, AB, Canada.
  • Alkelai A; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Antonarakis SE; Institute for Genomic Medicine, Columbia University Medical Center, New York, NY, USA.
  • Atallah I; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.
  • Bar-Yosef O; Division of Genetic Medicine, Lausanne University Hospital, Lausanne, Switzerland.
  • Bilan F; Pediatric Neurology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  • Bjorgo K; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Blanc X; CHU de Poitiers, Service de Génétique, EA3808 NEUVACOD, Poitiers, France.
  • Van Bogaert P; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  • Bolkier Y; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.
  • Burrage LC; CHU d'Angers, Service de Pédiatrie, EA3808 NEUVACOD, Angers, France.
  • Christ BU; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Granadillo JL; Pediatric Cardiology Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  • Dickson P; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Donald KA; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, SA, South Africa.
  • Dubourg C; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.
  • Eliyahu A; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.
  • Emrick L; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, SA, South Africa.
  • Engleman K; Service de Génétique Moléculaire et Génomique, CHU, Rennes, France.
  • Gonfiantini MV; University of Rennes, CNRS, IGDR, UMR 6290, Rennes, France.
  • Good JM; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Kalser J; The Danek Gertner Insitute of Human Genetics, Sheba Medical Center, Tel-Hahsomer, Israel.
  • Kloeckner C; Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hahsomer, Israel.
  • Lachmeijer G; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Macchiaiolo M; Center for Pediatric Genomic Medicine, Children's Mercy Hospital, Kansas City, MO, USA.
  • Nicita F; Rare Diseases and Medical Genetic Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Odent S; Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.
  • O'Heir E; Pediatric Neurology, Lausanne University Hospital, Lausanne, Switzerland.
  • Ortiz-Gonzalez X; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Pacio-Miguez M; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Palomares-Bralo M; Rare Diseases and Medical Genetic Unit, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Pena L; Unit of Neuromuscular and Neurodegenerative Diseases, Department of Neurosciences and Neurorehabilitation, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Platzer K; Service de Génétique Clinique, Centre de référence "Maladies Rares" Anomalies du développement CLAD-Ouest, Hôpital SUD, Échirolles, France.
  • Quinodoz M; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.
  • Ranza E; Center for Mendelian Genomics and Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Rosenfeld JA; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Roulet-Perez E; Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Santani A; Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, IdiPAZ, CIBERER, ISCIII, Madrid, Spain.
  • Santos-Simarro F; Cincinnati Children's Hospital and Medical Center Cincinnati, Cincinnati, OH, USA.
  • Pode-Shakked B; University of Cincinnati College of Medicine Cincinnati, Cincinnati, OH, USA.
  • Skraban C; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
  • Slaugh R; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
  • Superti-Furga A; Department of Ophthalmology, University of Basel, Basel, Switzerland.
  • Thiffault I; Medigenome, Swiss Institute of Genomic Medicine, Geneva, Switzerland.
  • van Jaabrsveld RH; Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Genet Med ; 23(10): 2016, 2021 Oct.
Article en En | MEDLINE | ID: mdl-34522029
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos