ArticleHuman genetics2019
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3.
Xueshan Xiao et al.PubMed ↗Full text ↗Publisher ↗
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ArticleHuman genetics2019
Xueshan Xiao et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.