Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia

10.1371/journal.pone.0072518

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Bibliographic Details
Main Authors:	Dave A., Laurie K., Staffieri S.E., Taranath D., Mackey D.A., Mitchell P., Wang J.J., Craig J.E., Burdon K.P., Sharma S.
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2019
Subjects:	ephrin A1 ephrin A5 article Australia autophosphorylation congenital cataract EPHA2 gene exome exon family history gene gene mutation gene sequence genetic disorder genetic screening genetic variability haplotype human microsatellite marker missense mutation phenotype population research protein domain protein motif protein phosphorylation protein protein interaction sequence alignment sequence analysis signal transduction single nucleotide polymorphism South Eastern Australia Cataract Cohort Studies Family Female Gene Frequency Genetic Diseases, Inborn Genetic Predisposition to Disease Humans Male Pedigree Point Mutation Receptor, EphA2
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/161273
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Institution:	National University of Singapore

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