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