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Commentary: Galactosemia Diagnosis by Whole Exome Sequencing Later in Life.
Friedman, Jennifer; Lucas-Del-Pozo, Sara; Moreno-Martinez, David; Camprodon-Gomez, Maria; Moreno-Martinez, Daniel; Hernandez-Vara, Jorge; Kurian, Manju A.
Afiliación
  • Friedman J; Department of Neurosciences and Pediatrics University of California Los Angeles California USA.
  • Lucas-Del-Pozo S; Department of Neurology Rady Children's Hospital Encinitas California USA.
  • Moreno-Martinez D; Rady Children's Institute for Genomic Medicine San Diego California USA.
  • Camprodon-Gomez M; Neurodegenerative Diseases Research Group, Vall Hebron Research Institute Vall Hebron University Hospital Barcelona Spain.
  • Moreno-Martinez D; Department of Clinical and Movement Neurosciences University College London Queen Square Institute of Neurology London United Kingdom.
  • Hernandez-Vara J; Lysosomal Storage Disorders Unit Royal Free Hospital National Health Service Foundation Trust and University College London London United Kingdom.
  • Kurian MA; Rare Diseases and Inborn Errors of Metabolism Unit Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona Barcelona Spain.
Mov Disord Clin Pract ; 8(Suppl 1): S40-S41, 2021 Aug.
Article en En | MEDLINE | ID: mdl-34514047
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Mov Disord Clin Pract Año: 2021 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Mov Disord Clin Pract Año: 2021 Tipo del documento: Article Pais de publicación: Estados Unidos