Associated Papers
Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.
Zhang KL et al.
Pediatric Research, 2025
Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome.
Ling C et al.
Bmc Medical Genetics, 2019
30642278 (PubMed )
Supplement: 12881_2018_725_MOESM4_ESM.xlsx › Sheet1
Molecular genetics of congenital nuclear cataract.
Deng H et al.
European Journal of Medical Genetics, 2014
X-linked cataract and Nance-Horan syndrome are allelic disorders.
Coccia M et al.
Human Molecular Genetics, 2009
Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Gómez-Laguna L et al.
Ophthalmic Genetics, 0
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