A start codon mutation of the TSPAN12 gene in Chinese families causes clinical heterogeneous familial exudative vitreoretinopathy

BACKGROUND: Familial exudative vitreoretinopathy (FEVR) is a severe clinically and genetically heterogeneous retinal disorder characterized with failure of vascular development of the peripheral retina. The symptoms of FEVR vary widely among patients in the same family, and even between the two eyes...

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Detalles Bibliográficos
Autores principales: Li, Wei, Wang, Ziwei, Sun, Yan, Wang, Zhuoshi, Bai, Jinyue, Xing, Bo, Sun, Xiao, Wang, Lusheng, Li, Jiankang, He, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785457/
https://www.ncbi.nlm.nih.gov/pubmed/31452356
http://dx.doi.org/10.1002/mgg3.948

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785457/
https://www.ncbi.nlm.nih.gov/pubmed/31452356
http://dx.doi.org/10.1002/mgg3.948

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