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pro vyhledávání: '"Paul K. Peprah"'
Autor:
Alshaima’a M. Qunies, Brittany D. Spitznagel, Yu Du, Paul K. Peprah, Yasmeen K. Mohamed, C. David Weaver, Kyle A. Emmitte
Publikováno v:
Molecules, Vol 29, Iss 11, p 2437 (2024)
Gain-of-function mutations in the KCNT1 gene, which encodes the sodium-activated potassium channel known as SLACK, are associated with the rare but devastating developmental and epileptic encephalopathy known as epilepsy of infancy with migrating foc
Externí odkaz:
https://doaj.org/article/0f2c5566b05b4d4bb6e0881d09280aae
