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Article

CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa

1 Apr 2008

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18387594
DOI: 10.1016/j.ajhg.2008.01.021

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CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis PigmentosaPMID 18387594Read ↗

The <i>CC2D1A</i>, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationSemantic proximity Read ↗

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