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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 06/2019, Volume 60, Issue 7, pp. 2659 - 2666
PURPOSE. The purpose of this study was to investigate the genetic mutation spectrum in Chinese patients with familial exudative vitreoretinopathy-associated... 
next-generation sequencing | FZD4 | genetic mutation spectrum | SURGICAL OUTCOMES | CLINICAL-FEATURES | IDENTIFICATION | TSPAN12 | genotype-phenotype association | rhegmatogenous retinal detachment | ZNF408 | GENES | OPHTHALMOLOGY | LRP5 MUTATIONS | familial exudative vitreoretinopathy | NDP | CHINESE PATIENTS
Journal Article
Journal Article
Journal Article
OPHTHALMIC SURGERY LASERS & IMAGING RETINA, ISSN 2325-8160, 02/2019, Volume 50, Issue 2, pp. 120 - 124
Familial exudative vitreoretinopathy (FEVR) is a rare hereditary ocular disorder characterized by incomplete or abnormal development of peripheral retinal... 
SURGERY | NORRIE-DISEASE | ZNF408 | FZD4 | LRP5 | OPHTHALMOLOGY | RETINOPATHY | RETINA | MUTATIONS | TSPAN12 | IDENTIFICATION | Retinal Diseases - genetics | Genetic Predisposition to Disease | Pedigree | Humans | Child, Preschool | Male | Penetrance | Eye Proteins - genetics | Mutation | Genetic Diseases, X-Linked | Nerve Tissue Proteins - genetics | Eye Diseases, Hereditary - genetics
Journal Article
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 01/2019, Volume 7, Issue 1, pp. e00503 - n/a
Journal Article
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