ArticleHuman mutation2020
Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation.
Nicole Weisschuh et al.PubMed ↗Full text ↗Publisher ↗
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ArticleHuman mutation2020
Nicole Weisschuh et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.