Associated Papers
Genetic spectrum of congenital cataract with optional ocular and multisystem abnormalities.
Zhang H et al.
Bmc Medical Genomics, 2025
Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.
Zhang KL et al.
Pediatric Research, 2025
Genome sequencing reveals novel variants in a diverse population with congenital anterior segment anomalies.
Hussain A et al.
Scientific Reports, 2025
Great clinical variability of Nance Horan syndrome due to deleterious NHS mutations in two unrelated Spanish families.
Hernández V et al.
Ophthalmic Genetics, 2019
Congenital diaphragmatic hernia as a part of Nance-Horan syndrome?
Kammoun M et al.
European Journal of Human Genetics : Ejhg, 2018
Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS gene.
Sun W et al.
Plos One, 2014
Mutation analysis of 12 genes in Chinese families with congenital cataracts.
Sun W et al.
Molecular Vision, 2011
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