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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 19, 2024. (Total: 231613Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Photophobia and CNGA3[original query]
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia.
European journal of human genetics : EJHG 2005 Mar 13 (3): 302-8.
Kohl Susanne, Varsanyi Balazs, Antunes Gesine Abadin, Baumann Britta, Hoyng Carel B, Jägle Herbert, Rosenberg Thomas, Kellner Ulrich, Lorenz Birgit, Salati Roberto, Jurklies Bernhard, Farkas Agnes, Andreasson Sten, Weleber Richard G, Jacobson Samuel G, Rudolph Günther, Castellan Claudio, Dollfus Helene, Legius Eric, Anastasi Mario, Bitoun Pierre, Lev Dorit, Sieving Paul A, Munier Francis L, Zrenner Eberhart, Sharpe Lindsay T, Cremers Frans P M, Wissinger Ber
Novel CNGA3 mutations in Chinese patients with achromatopsia.
The British journal of ophthalmology 2015 Apr 99 (4): 571-6.
Liang Xiaofang, Dong Fangtian, Li Hui, Li Huajin, Yang Lizhu, Sui Ruifa
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