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Assessment of ataxia phenotype in a new mouse model of galactose-1 phosphate uridylyltransferase (GALT) deficiency.
Chen, Wyman; Caston, Rose; Balakrishnan, Bijina; Siddiqi, Anwer; Parmar, Kamalpreet; Tang, Manshu; Feng, Merry; Lai, Kent.
Afiliação
  • Chen W; Department of Pediatrics, University of Utah School of Medicine, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
  • Caston R; Department of Pediatrics, University of Utah School of Medicine, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
  • Balakrishnan B; Dartmouth College, Hanover, NH, USA.
  • Siddiqi A; Department of Pediatrics, University of Utah School of Medicine, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
  • Parmar K; Department of Pathology and Laboratory Medicine, University of Florida College of Medicine, Jacksonville, FL, USA.
  • Tang M; Department of Pathology and Laboratory Medicine, University of Florida College of Medicine, Jacksonville, FL, USA.
  • Feng M; Department of Pediatrics, University of Utah School of Medicine, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
  • Lai K; Department of Pediatrics, University of Utah School of Medicine, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
J Inherit Metab Dis ; 40(1): 131-137, 2017 01.
Article em En | MEDLINE | ID: mdl-27783170

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Galactosemias / UDPglucose-Hexose-1-Fosfato Uridiltransferase Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Galactosemias / UDPglucose-Hexose-1-Fosfato Uridiltransferase Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article