Author:
Andreux F.,Hantaï D.,Eymard B.
Subject
Clinical Neurology,Neurology
Reference101 articles.
1. A common mutation (1267delG) in congenital myasthenic patients of Gipsy ethnic origin;Abicht;Neurology,1999
2. Genetic analysis of the entire AChR epsilon subunit gene in 52 congenital myasthenic families;Abicht;Acta Myol,2000
3. Congenital Lambert-Eaton myasthenic syndrome;Bady;J Neurol Neurosurg Psychiatry,1987
4. Myopathy, myasthenic syndrome, and epidermolysis bullosa simplex due to plectin deficiency;Banwell;J Neuropathol Exp Neurol,1999
5. Congenital myasthenic syndrome due to two novel mutations in the acetylcholine receptor epsilon subunit gene;Brengman;Muscle Nerve,1998
Cited by
8 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献