Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sonia M. Hasan"'
Autor:
Zeynep S. Karalok, Alfredo Megaro, Marta Cenciarini, Alev Guven, Sonia M. Hasan, Birce D. Taskin, Paola Imbrici, Serdar Ceylaner, Mauro Pessia, Maria C. D'Adamo
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Episodic ataxia type 1 (EA1), a Shaker-like K+channelopathy, is a consequence of genetic anomalies in the KCNA1 gene that lead to dysfunctions in the voltage-gated K+ channel Kv1. 1. Generally, KCNA1 mutations are inherited in an autosomal dominant m
Externí odkaz:
https://doaj.org/article/8168914858c945798b7177c59a8efaed
Autor:
Nugroho, Puguh Setyo1 mailto:puguh-s-n@fk.unair.ac.id, Falerina, Rosa1, Perdana, Rizka Fathoni2,3, Faizah, Zakiyatul4, Fathoni, Azhar Nur5, Kurniawan, Agde Muzaky4, Arsy, Danial Habri4
Publikováno v:
Jurnal Layanan Masyarakat. 2023, Vol. 7 Issue 4, p490-502. 13p.
Publikováno v:
Pharma Science Monitor. Jul-Sep2017, Vol. 8 Issue 3, p17-25. 9p.
Autor:
Karalok, Zeynep S., Megaro, Alfredo, Cenciarini, Marta, Guven, Alev, Hasan, Sonia M., Taskin, Birce D., Imbrici, Paola, Ceylaner, Serdar, Pessia, Mauro, D'Adamo, Maria C.
Publikováno v:
Frontiers in Neurology; 7/25/2018, pN.PAG-N.PAG, 5p
Publikováno v:
Neurochemical Research; Jul2007, Vol. 32 Issue 7, p1169-1178, 10p