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NXG.0000000000000182
NXG.0000000000000182
http://dx.doi.org/10.1212/NXG.0000000000000182
A novel intronic mutation in MTM1 detected by RNA analysis in a case of X-linked myotubular myopathy.
P356
Q41514620-75C5A052-C469-4F4B-BF60-FA1E7D0C958A
P356
NXG.0000000000000182
http://dx.doi.org/10.1212/NXG.0000000000000182