Genetic landscape of FOXC2 mutations in lymphedema-distichiasis syndrome: Different mechanism of pathogenicity for mutations in different domains-Reference-Cited by-同舟云学术

Genetic landscape of FOXC2 mutations in lymphedema-distichiasis syndrome: Different mechanism of pathogenicity for mutations in different domains

Published:2022-09 Issue: Volume:222 Page:109136
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Jiang Lingxi,Ren Weiming,Xie Chunbao,Duan Suyang,Dai Chao,Wei Yao,Luo Dongyan,Wang Tingting,Gong Bo,Liu Xiaoqi,Yang Zhenglin,Ye Zimeng,Chen Hui,Shi Yi^ORCID

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference39 articles.

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4. The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis;Berry;Hum. Mol. Genet.,2005

5. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24;Brice;J. Med. Genet.,2002

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