Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy-Reference-Cited by-同舟云学术

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Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

Published:2016-03 Issue:3 Volume:98 Page:592
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Poulter James A.,Ali Manir,Gilmour David F.,Rice Aine,Kondo Hiroyuki,Hayashi Kenshi,Mackey David A.,Kearns Lisa S.,Ruddle Jonathan B.,Craig Jamie E.,Pierce Eric A.,Downey Louise M.,Mohamed Moin D.,Markham Alexander F.,Inglehearn Chris F.,Toomes Carmel

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Early onset high myopia and severe anisometropia associated with familial exudative vitreoretinopathy of irregular dominant inheritance in 12 Chinese families：analysis of refraction features and pathogenic variations;2024-01-31

2. Mutation spectrum in a cohort with familial exudative vitreoretinopathy;Molecular Genetics & Genomic Medicine;2022-07-25

3. Reaching a FEVR Pitch: A Case Series of Familial Exudative Vitreoretinopathy in Northern Ireland;Journal of Pediatric Ophthalmology & Strabismus;2021-09

4. Novel mutation in TSPAN12 associated with familial exudative vitreoretinopathy in a Chinese pedigree;Ophthalmic Genetics;2021-08-27

5. Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy;Genes;2021-06-27

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