Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations
Author:
Affiliation:
1. Department of Molecular Reproduction, Development and Genetics Indian Institute of Science Bangalore India
2. Minto Ophthalmic Hospital Bangalore India
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810490498198
Reference12 articles.
1. Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2
2. All kinesin superfamily protein, KIF, genes in mouse and human
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