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Gain-of-function mutation in the voltage-gated potassium channel gene KCNQ1 and glucose-stimulated hypoinsulinemia - case report

BACKGROUND: The voltage-gated potassium channel Kv7.1 encoded by KCNQ1 is located in both cardiac myocytes and insulin producing beta cells. Loss-of-function mutations in KCNQ1 causes long QT syndrome along with glucose-stimulated hyperinsulinemia, increased C-peptide and postprandial hypoglycemia....

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Detalhes bibliográficos
Publicado no:BMC Endocr Disord
Main Authors: Zhang, Jinyi, Juhl, Christian R., Hylten-Cavallius, Louise, Salling-Olsen, Morten, Linneberg, Allan, Holst, Jens Juul, Hansen, Torben, Kanters, Jørgen K., Torekov, Signe S.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7069191/
https://ncbi.nlm.nih.gov/pubmed/32164657
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12902-020-0513-x
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