Genetic research on Nance-Horan syndrome caused by a new novel in the NHS
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference43 articles.
1. Inherited cataracts: molecular genetics, clinical features, disease mechanisms and novel therapeutic approaches;Berry;Br J Ophthalmol.,2020
2. The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females;Bixler;Clin Genet.,1984
3. The Nance-Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphology;Brooks;Hum Mol Genet.,2010
4. Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation;Burdon;Am J Hum Genet.,2003
5. Casto C, Dipasquale V, Ceravolo I, et al. Prominent and Regressive Brain Developmental Disorders Associated with Nance-Horan Syndrome. Brain Sci. 2021;11(9):1150. Published 2021 Aug 29. doi:10.3390/brainsci11091150
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