A mutation of the acetylcholine receptor (AChR) epsilon subunit (ε1267delG) is a frequent cause for sporadic and autosomal recessive congenital myasthenic syndromes (CMS)

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作者：
Abicht, A
Karcagi, V
Herczegfalvi, A
Mortier, W
Müller-Felber, W
Pongratz, D
Rüdel, R
Lochmuller, H
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NEUROLOGY | 1999年 / 52卷 / 06期
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R74 [神经病学与精神病学];
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页码：A184 / A184
页数：1
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