CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES-Reference-Cited by-同舟云学术

CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES

Published:2019-06 Issue:6 Volume:39 Page:1186-1199
ISSN:0275-004X
Container-title:Retina
language:en
Short-container-title:

Author:

Talib Mays,van Schooneveld Mary J.,Thiadens Alberta A.,Fiocco Marta,Wijnholds Jan,Florijn Ralph J.,Schalij-Delfos Nicoline E.,van Genderen Maria M.,Putter Hein,Cremers Frans P. M.,Dagnelie Gislin,ten Brink Jacoline B.,Klaver Caroline C. W.,van den Born L. Ingeborgh,Hoyng Carel B.,Bergen Arthur A.,Boon Camiel J. F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology,General Medicine

Reference44 articles.

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2. Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype-phenotype correlations and impact on genetic counseling;Pelletier;Hum Mutat,2007

3. RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections;Zito;J Med Genet,2003

4. Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations;Sandberg;Invest Ophthalmol Vis Sci,2007

5. Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa;Flaxel;Br J Ophthalmol,1999

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