ArticleNeurology2012
A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1.
D L Raja Rayan et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleNeurology2012
D L Raja Rayan et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.