Potassium channel

KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects
Chiao Xin Lim, Michael G Ricos, Leanne M Dibbens, Sarah E Heron

Journal of Medical Genetics Apr 2016, 53 (4) 217-225; DOI: 10.1136/jmedgenet-2015-103508
KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability
Namik Kaya, Maysoon Alsagob, Maria Cristina D'Adamo, Albandary Al-Bakheet, Sonia Hasan, Maria Muccioli, Faten B Almutairi, Rawan Almass, Mazhor Aldosary, Dorota Monies, Osama M Mustafa, Banan Alyounes, Rosan Kenana, Jawaher Al-Zahrani, Eva Naim, Faisal S Binhumaid, Alya Qari, Fatema Almutairi, Brian Meyer, Timothy F Plageman, Mauro Pessia, Dilek Colak, Mohammed Al-Owain

Journal of Medical Genetics Nov 2016, 53 (11) 786-792; DOI: 10.1136/jmedgenet-2015-103637

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Potassium channel