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NXG.0000000000000168
NXG.0000000000000168
http://dx.doi.org/10.1212/NXG.0000000000000168
Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy.
P356
Q33879396-7BC0196E-66F2-474B-A930-47FAC4E548F8
P356
NXG.0000000000000168
http://dx.doi.org/10.1212/NXG.0000000000000168