ArticleChannels (Austin, Tex.)2019
Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy.
Melissa T Carter et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
21 papers cite it
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ArticleChannels (Austin, Tex.)2019
Melissa T Carter et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.