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Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.
Allocco, August A; Jin, Sheng Chih; Duy, Phan Q; Furey, Charuta G; Zeng, Xue; Dong, Weilai; Nelson-Williams, Carol; Karimy, Jason K; DeSpenza, Tyrone; Hao, Le T; Reeves, Benjamin; Haider, Shozeb; Gunel, Murat; Lifton, Richard P; Kahle, Kristopher T.
Afiliación
  • Allocco AA; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Jin SC; Department of Genetics, School of Medicine, Yale University, New Haven, CT, United States.
  • Duy PQ; Laboratory of Human Genetics and Genomics, The Rockefeller University, New York, NY, United States.
  • Furey CG; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Zeng X; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Dong W; Department of Genetics, School of Medicine, Yale University, New Haven, CT, United States.
  • Nelson-Williams C; Laboratory of Human Genetics and Genomics, The Rockefeller University, New York, NY, United States.
  • Karimy JK; Department of Genetics, School of Medicine, Yale University, New Haven, CT, United States.
  • DeSpenza T; Department of Genetics, School of Medicine, Yale University, New Haven, CT, United States.
  • Hao LT; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Reeves B; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Haider S; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Gunel M; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
  • Lifton RP; Department of Computational Chemistry, University College London School of Pharmacy, London, United Kingdom.
  • Kahle KT; Department of Neurosurgery, School of Medicine, Yale University, New Haven, CT, United States.
Front Cell Neurosci ; 13: 425, 2019.
Article en En | MEDLINE | ID: mdl-31616254

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Cell Neurosci Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Cell Neurosci Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza