Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family: A case report

INTRODUCTION: Severe myopic anisometropia has been identified to have heritability, but the pathogenesis of anisometropia still remains obscure. CASE DESCRIPTION: Here, we presented a Chinese severe myopic anisometropia family with 5 members affected. Though using the exome sequencing, we identified...

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Detalles Bibliográficos
Autores principales: Feng, Lei, Zhou, Daizhan, Zhang, Zhou, He, Lin, Liu, Yun, Yang, Yabo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478323/
https://www.ncbi.nlm.nih.gov/pubmed/28614238
http://dx.doi.org/10.1097/MD.0000000000007138

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478323/
https://www.ncbi.nlm.nih.gov/pubmed/28614238
http://dx.doi.org/10.1097/MD.0000000000007138

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