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The American Journal of Human Genetics, ISSN 0002-9297, 09/2013, Volume 93, Issue 3, pp. 571 - 578
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 10/2016, Volume 233, Issue 10, pp. 1124 - 1141
Journal Article
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 10/2016, Volume 233, Issue 10, pp. 1124 - 1141
Journal Article
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 05/2019, Volume 60, Issue 6, pp. 2347 - 2356
PURPOSE. To define characteristic ocular features in a group of patients with autosomal recessive (AR) PROM1 cone-rod dystrophy (CRD). METHODS. Three males and... 
RETINAL DEGENERATION | PCDH21 | PHENOTYPE | CLINICAL CHARACTERISTICS | IDENTIFICATION | CDHR1 GENE | fundus autofluorescence | CDHR1 | electroretinogram | OPHTHALMOLOGY | cone-rod dystrophy | FRAMESHIFT MUTATION | PROM1 | RETINITIS-PIGMENTOSA | SEQUENCING REVEALS | PROGRESSION | Genetics
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 11/2017, Volume 255, Issue 11, pp. 2099 - 2111
Journal Article
Journal Article