Associated Papers
Structural analysis of missense mutations occurring in the DNA-binding domain of HSF4 associated with congenital cataracts.
Xiao Z et al.
Journal of Structural Biology: X, 2020
Genetic landscape of isolated pediatric cataracts: extreme heterogeneity and variable inheritance patterns within genes.
Reis LM et al.
Human Genetics, 2019
Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family.
Jiao X et al.
Plos One, 2019
A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family.
Berry V et al.
Eye (london, England), 2018
Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.
Anand D et al.
Human Mutation, 2018
A novel homozygous mutation in HSF4 causing autosomal recessive congenital cataract.
Behnam M et al.
Journal of Human Genetics, 2016
HSF4 promotes G1/S arrest in human lens epithelial cells by stabilizing p53.
Huang M et al.
Biochimica Et Biophysica Acta, 2015
A novel HSF4 gene mutation causes autosomal-dominant cataracts in a Chinese family.
Lv H et al.
G3 (bethesda, Md.), 2014
Select a paper to view details