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Publications by OV Evgrafov
Mutation in the Connexin 50 Gene (GJA8) in a Russian Family With Zonular Pulverulent Cataract
Clinical Genetics
Genetics
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A 5-Base Insertion in the γC-crystallin Gene Is Associated With Autosomal Dominant Variable Zonular Pulverulent Cataract
Human Genetics
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Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family With Autosomal Dominant Pulverulent Cataract
Molecular Syndromology
Genetics
Novel Mutation in GJB4 Gene (Connexin 30.3) in a Family With Erythrokeratodermia Variabilis
Acta Dermato-Venereologica
Dermatology
Medicine
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
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Uni-Ocular Zonular Cataract
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
Identification and Functional Analysis of a Novel MIP Gene Mutation Associated With Congenital Cataract in a Chinese Family
PLoS ONE
Multidisciplinary
Unique Presentation of Congenital Cataract Concurrent With Microcornea, Microphthalmia Plus Posterior Capsule Defect in Monozygotic Twins Caused by a Novel GJA8 Mutation
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
KID Syndrome: Report of a Scandinavian Patient With Connexin‐26 Gene Mutation
Acta Dermato-Venereologica
Dermatology
Medicine
