학술논문
CONGENITAL MUSCULAR DYSTROPHIES: EP.70 Exploring the role of genetic modifiers in a mild LAMA2-RD case associated with a LAMA2 loss-of-function mutation
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Abstract
Author
Source
In Neuromuscular Disorders October 2021 31 Supplement 1:S70-S70
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Language
ISSN
0960-8966