CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders

Author:

Wissinger Bernd,Gamer Daphne,Jägle Herbert,Giorda Roberto,Marx Tim,Mayer Simone,Tippmann Sabine,Broghammer Martina,Jurklies Bernhard,Rosenberg Thomas,Jacobson Samuel G.,Sener E. Cumhur,Tatlipinar Sinan,Hoyng Carel B.,Castellan Claudio,Bitoun Pierre,Andreasson Sten,Rudolph Günter,Kellner Ulrich,Lorenz Birgit,Wolff Gerhard,Verellen-Dumoulin Christine,Schwartz Marianne,Cremers Frans P.M.,Apfelstedt-Sylla Eckart,Zrenner Eberhart,Salati Roberto,Sharpe Lindsay T.,Kohl Susanne

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference37 articles.

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3. Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene;Ayyagari;Mol Vis,1999

4. Selective loss of of cone function in mice lacking the cyclic nucleotide-gated channel CNG3;Biel;Proc Natl Acad Sci USA,1999

5. Another member of the cyclic nucleotide-gated channel family, expressed in testis, kidney, and heart;Biel;Proc Natl Acad Sci USA,1994

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