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Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract. (2018)

First Author: Berry V

Attributed to: Imputation-aided analysis of DNA methylomes funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41433-018-0154-8

PubMed Identifier: 29934635

Publication URI: http://europepmc.org/abstract/MED/29934635

Type: Journal Article/Review

Volume: 32

Parent Publication: Eye (London, England)

Issue: 10

ISSN: 0950-222X