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
Personalized diagnosis and management of congenital cataract by next-generation sequencing.
Gillespie RL et al.
Ophthalmology, 2014
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