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Heterozygous Monocarboxylate Transporter 1 (MCT1, SLC16A1) Deficiency as a Cause of Recurrent Ketoacidosis.
Balasubramaniam, Shanti; Lewis, Barry; Greed, Lawrence; Meili, David; Flier, Annegret; Yamamoto, Raina; Bilic, Karmen; Till, Claudia; Sass, Jörn Oliver.
Afiliação
  • Balasubramaniam S; Metabolic Unit, Department of Rheumatology and Metabolic Medicine, Princess Margaret Hospital, Perth, WA, Australia.
  • Lewis B; School of Paediatrics and Child Health, University of Western Australia, Perth, WA, Australia.
  • Greed L; PathWest Laboratories WA, Princess Margaret Hospital, Perth, WA, Australia.
  • Meili D; PathWest Laboratories WA, Princess Margaret Hospital, Perth, WA, Australia.
  • Flier A; Clinical Chemistry & Biochemistry, University Children's Hospital, Zürich, Switzerland.
  • Yamamoto R; Clinical Chemistry & Biochemistry, University Children's Hospital, Zürich, Switzerland.
  • Bilic K; Medizinisches Versorgungszentrum, Dr Eberhard & Partner, Dortmund, Germany.
  • Till C; Clinical Institute of Laboratory Diagnostics, University Hospital Center Zagreb, Zagreb, Croatia.
  • Sass JO; Bioanalytics & Biochemistry, Department of Natural Sciences, Bonn-Rhein-Sieg University of Applied Sciences, von-Liebig-Str. 20, 53359, Rheinbach, Germany.
JIMD Rep ; 29: 33-38, 2016.
Article em En | MEDLINE | ID: mdl-26608392
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália