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Congenital hyperinsulinism due to mutations in HNF1A.
Yau, Daphne; Colclough, Kevin; Natarajan, Anuja; Parikh, Ruchi; Canham, Natalie; Didi, Mohammed; Senniappan, Senthil; Banerjee, Indraneel.
Afiliación
  • Yau D; Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK. Electronic address: daphne.yau@mail.mcgill.ca.
  • Colclough K; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK.
  • Natarajan A; Doncaster Royal Infirmary, Doncaster, UK.
  • Parikh R; Paediatric Endocrinology, Alder Hey Children's Hospital, Liverpool, UK.
  • Canham N; Liverpool Women's Hospital, Liverpool, UK.
  • Didi M; Paediatric Endocrinology, Alder Hey Children's Hospital, Liverpool, UK.
  • Senniappan S; Paediatric Endocrinology, Alder Hey Children's Hospital, Liverpool, UK.
  • Banerjee I; Department of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK.
Eur J Med Genet ; 63(6): 103928, 2020 Jun.
Article en En | MEDLINE | ID: mdl-32325224
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hiperinsulinismo Congénito / Factor Nuclear 1-alfa del Hepatocito Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hiperinsulinismo Congénito / Factor Nuclear 1-alfa del Hepatocito Tipo de estudio: Prognostic_studies Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article