Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Morten Salling-Olsen"'
Autor:
Jinyi Zhang, Christian R. Juhl, Louise Hylten-Cavallius, Morten Salling-Olsen, Allan Linneberg, Jens Juul Holst, Torben Hansen, Jørgen K. Kanters, Signe S. Torekov
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract 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 hyperinsuli
Externí odkaz:
https://doaj.org/article/69ea9bc057dc4782a9935440cb68bf8d
Autor:
Christian R. Juhl, Jørgen K. Kanters, Jens J. Holst, Signe S. Torekov, Jinyi Zhang, Torben Hansen, Allan Linneberg, Morten Salling-Olsen, Louise Hyltén-Cavallius
Publikováno v:
Zhang, J, Juhl, C R, Hylten-Cavallius, L, Salling-Olsen, M, Linneberg, A, Holst, J J, Hansen, T, Kanters, J K & Torekov, S S 2020, ' Gain-of-function mutation in the voltage-gated potassium channel gene KCNQ1 and glucose-stimulated hypoinsulinemia-case report ', B M C Endocrine Disorders, vol. 20, 38 . https://doi.org/10.1186/s12902-020-0513-x
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-5 (2020)
BMC Endocrine Disorders
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-5 (2020)
BMC Endocrine Disorders
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, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b2c2088e9bea25547f3fd14a38ef94a
https://curis.ku.dk/ws/files/245667108/s12902_020_0513_x.pdf
https://curis.ku.dk/ws/files/245667108/s12902_020_0513_x.pdf
