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Structural basis for early-onset neurological disorders caused by mutations in human selenocysteine synthase.
Puppala, Anupama K; French, Rachel L; Matthies, Doreen; Baxa, Ulrich; Subramaniam, Sriram; Simonovic, Miljan.
Afiliação
  • Puppala AK; Department of Biochemistry an Molecular Genetics, University of Illinois at Chicago, Chicago, Illinois 60607, USA.
  • French RL; Department of Biochemistry an Molecular Genetics, University of Illinois at Chicago, Chicago, Illinois 60607, USA.
  • Matthies D; Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Baxa U; Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Subramaniam S; Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Simonovic M; Department of Biochemistry an Molecular Genetics, University of Illinois at Chicago, Chicago, Illinois 60607, USA.
Sci Rep ; 6: 32563, 2016 08 31.
Article em En | MEDLINE | ID: mdl-27576344

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ataxia / Convulsões / RNA de Transferência / Selenocisteína / Aminoacil-tRNA Sintetases / Espasticidade Muscular Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ataxia / Convulsões / RNA de Transferência / Selenocisteína / Aminoacil-tRNA Sintetases / Espasticidade Muscular Idioma: En Ano de publicação: 2016 Tipo de documento: Article