Your browser doesn't support javascript.
loading
Molecular mechanisms of congenital hyperinsulinism due to autosomal dominant mutations in ABCC8.
Nessa, Azizun; Aziz, Qadeer H; Thomas, Alison M; Harmer, Stephen C; Tinker, Andrew; Hussain, Khalid.
Afiliación
  • Nessa A; Genetics and Genomic Medicine, UCL Institute of Child Health, London WC1N 1EH, UK.
  • Aziz QH; The Heart Centre, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK and.
  • Thomas AM; The Heart Centre, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK and.
  • Harmer SC; The Heart Centre, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK and.
  • Tinker A; The Heart Centre, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK and.
  • Hussain K; Genetics and Genomic Medicine, UCL Institute of Child Health, London WC1N 1EH, UK, Genetics and Genomic Medicine, UCL Institute of Child Health, London Centre for Paediatric Endocrinology and Metabolism, Great Ormond Street Hospital for Children NHS, London WC1N 1EH, UK khalid.hussain@ucl.ac.uk.
Hum Mol Genet ; 24(18): 5142-53, 2015 Sep 15.
Article en En | MEDLINE | ID: mdl-26092864
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hiperinsulinismo Congénito / Receptores de Sulfonilureas / Genes Dominantes / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male / Newborn Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hiperinsulinismo Congénito / Receptores de Sulfonilureas / Genes Dominantes / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Male / Newborn Idioma: En Año: 2015 Tipo del documento: Article