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Congenital valvular defects associated with deleterious mutations in the PLD1 gene.
Ta-Shma, Asaf; Zhang, Kai; Salimova, Ekaterina; Zernecke, Alma; Sieiro-Mosti, Daniel; Stegner, David; Furtado, Milena; Shaag, Avraham; Perles, Zeev; Nieswandt, Bernhard; Rein, Azaria J J T; Rosenthal, Nadia; Neiman, Aaron M; Elpeleg, Orly.
Afiliação
  • Ta-Shma A; Department of Pediatric Cardiology, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
  • Zhang K; Monique and Jacques Roboh Department of Genetic Research, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
  • Salimova E; Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, USA.
  • Zernecke A; Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
  • Sieiro-Mosti D; Institute of Experimental Biomedicine, University Hospital Würzburg, Würzburg, Germany.
  • Stegner D; Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
  • Furtado M; Institute of Experimental Biomedicine, University Hospital Würzburg, Würzburg, Germany.
  • Shaag A; Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
  • Perles Z; Monique and Jacques Roboh Department of Genetic Research, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
  • Nieswandt B; Department of Pediatric Cardiology, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
  • Rein AJ; Institute of Experimental Biomedicine, University Hospital Würzburg, Würzburg, Germany.
  • Rosenthal N; Department of Pediatric Cardiology, Hadassah, Hebrew University Medical Center, Jerusalem, Israel.
  • Neiman AM; Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria, Australia.
  • Elpeleg O; Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York, USA.
J Med Genet ; 54(4): 278-286, 2017 04.
Article em En | MEDLINE | ID: mdl-27799408
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfolipase D / Prolapso da Valva Mitral / Predisposição Genética para Doença / Doenças Genéticas Ligadas ao Cromossomo X / Cardiopatias Congênitas / Mixoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Med Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Israel
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfolipase D / Prolapso da Valva Mitral / Predisposição Genética para Doença / Doenças Genéticas Ligadas ao Cromossomo X / Cardiopatias Congênitas / Mixoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Med Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Israel