Haploinsufficiency ofRCBTB1is associated with Coats disease and familial exudative vitreoretinopathy-Reference-Cited by-全球学者库

Haploinsufficiency ofRCBTB1is associated with Coats disease and familial exudative vitreoretinopathy

Published:2016-02-11 Issue:8 Volume:25 Page:1637-1647
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Wu Jeng-Hung,Liu Jorn-Hon,Ko Yu-Chieh,Wang Chi-Tang,Chung Yu-Chien,Chu Kuo-Chang,Liu Tze-Tze,Chao Hsiao-Ming,Jiang Yun-Jin,Chen Shih-Jen,Chung Ming-Yi

Funder

Ministry of Science and Technology (MOST)

Cheng-Yang Collaborative Research Foundation

National Core Facility Program for Biotechnology

National Research Program for Biopharmaceuticals

National Health Research Institutes, Taiwan

Ministry of Science and Technology, Taiwan

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/25/8/1637/18527882/ddw041.pdf

Reference45 articles.

1. Familial Exudative Vitreoretinopathy

2. Fluorescein Angiographic Findings in Familial Exudative Vitreoretinopathy

3. Intrafamilial variability of the ocular phenotype in a Polish family with a missense mutation (A63D) in the Norrie disease gene

4. Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused byFZD4Mutations in two Distinct Pedigrees

5. The molecular basis of human retinal and vitreoretinal diseases

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