دورية أكاديمية

CHANNELOPATHIES AND RELATED DISORDERS: EP.225 Autosomal dominant early onset vacuolar myopathy with granular material, without periodic paralysis, associated with c.1583C>A CACNA1S gene mutation

التفاصيل البيبلوغرافية
العنوان: CHANNELOPATHIES AND RELATED DISORDERS: EP.225 Autosomal dominant early onset vacuolar myopathy with granular material, without periodic paralysis, associated with c.1583C>A CACNA1S gene mutation
المؤلفون: Bisciglia, M., Kadhim, H., Lecomte, S., Vandernoot, I., Desmyter, L., Remiche, G.
المصدر: In Neuromuscular Disorders October 2021 31 Supplement 1:S117-S118
قاعدة البيانات: ScienceDirect
الوصف
تدمد:09608966
DOI:10.1016/j.nmd.2021.07.249