A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms.
A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. — المؤلف: Sampedro Castañeda, Marisol — Brain : a journal of neurology 20190715
- المؤلف
- Sampedro Castañeda, Marisol
- النشر
- Brain : a journal of neurology 20190715
- الوصف
- 3308-3318 p.
- الموضوعات
- Animals؛ Child؛ Humans؛ Hypokalemic Periodic Paralysis؛ Male؛ Membrane Potentials؛ Muscle, Skeletal؛ Mutation, Missense