S-EPMC1735867 - A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance. - OmicsDI

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A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

ABSTRACT:

SUBMITTER: Burdon KP

PROVIDER: S-EPMC1735867 | biostudies-literature | 2004 Aug

REPOSITORIES: biostudies-literature