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Biallelic TOR1A variants in an infant with severe arthrogryposis.
Reichert, Sara Chadwick; Gonzalez-Alegre, Pedro; Scharer, Gunter H.
Afiliación
  • Reichert SC; Department of Medical Genetics and Genomics (S.C.R., G.H.S.), Children's Minnesota, Minneapolis; Department of Neurology (P.G.-A.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia; and Raymond G. Perelman Center for Cellular & Molecular Therapeutics (P.G.-A.), The Children's Hospital of Philadelphia, PA.
  • Gonzalez-Alegre P; Department of Medical Genetics and Genomics (S.C.R., G.H.S.), Children's Minnesota, Minneapolis; Department of Neurology (P.G.-A.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia; and Raymond G. Perelman Center for Cellular & Molecular Therapeutics (P.G.-A.), The Children's Hospital of Philadelphia, PA.
  • Scharer GH; Department of Medical Genetics and Genomics (S.C.R., G.H.S.), Children's Minnesota, Minneapolis; Department of Neurology (P.G.-A.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia; and Raymond G. Perelman Center for Cellular & Molecular Therapeutics (P.G.-A.), The Children's Hospital of Philadelphia, PA.
Neurol Genet ; 3(3): e154, 2017 Jun.
Article en En | MEDLINE | ID: mdl-28516161

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Neurol Genet Año: 2017 Tipo del documento: Article País de afiliación: Panamá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Neurol Genet Año: 2017 Tipo del documento: Article País de afiliación: Panamá