학술논문
NEW GENES AND DISEASES: EP.301 The alpha2-subunit of the AP2 clathrin adaptor as the causal gene in an atypical myopathy with granulofilamentous inclusions
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Abstract
Author
Source
In Neuromuscular Disorders October 2021 31 Supplement 1:S141-S142
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Language
ISSN
0960-8966