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SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus.
Jin, Sheng Chih; Furey, Charuta G; Zeng, Xue; Allocco, August; Nelson-Williams, Carol; Dong, Weilai; Karimy, Jason K; Wang, Kevin; Ma, Shaojie; Delpire, Eric; Kahle, Kristopher T.
Afiliação
  • Jin SC; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Furey CG; Laboratory of Human Genetics and Genomics, The Rockefeller University, New York, NY, USA.
  • Zeng X; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Allocco A; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Nelson-Williams C; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Dong W; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Karimy JK; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Wang K; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
  • Ma S; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Delpire E; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
  • Kahle KT; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
Mol Genet Genomic Med ; 7(9): e892, 2019 09.
Article em En | MEDLINE | ID: mdl-31393094
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aqueduto do Mesencéfalo / Simportadores / Doenças Genéticas Ligadas ao Cromossomo X / Hidrocefalia / Mutação Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aqueduto do Mesencéfalo / Simportadores / Doenças Genéticas Ligadas ao Cromossomo X / Hidrocefalia / Mutação Idioma: En Ano de publicação: 2019 Tipo de documento: Article