Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.

Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization. — المؤلف: Wang, Haicui — Brain : a journal of neurology 20171107

المؤلف
Wang, Haicui
النشر
Brain : a journal of neurology 20171107
الوصف
2838-2850 p.
الموضوعات
Animals؛ Animals, Genetically Modified؛ Atrophy؛ Axons؛ Brain؛ Caenorhabditis elegans؛ Caenorhabditis elegans Proteins؛ Child, Preschool