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ArticleAmerican journal of human genetics2001

CNGA3 mutations in hereditary cone photoreceptor disorders.

B Wissinger et al.PubMed ↗Full text ↗Publisher ↗

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138 papers cite itlatest 60 shown

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this papertrialcites it

The trial

NCT01648452phase 1/phase 25 enrolled2012
Full record →Abstract, authors, funding and every citing paper · PMID 11536077