ArticleOrphanet journal of rare diseases2014
Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
María J Aparisi et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
46 papers cite it
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ArticleOrphanet journal of rare diseases2014
María J Aparisi et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.