Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.
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BORIS DOI
Publisher DOI
PubMed ID
19200527
Description
Cone-rod dystrophies are inherited dystrophies of the retina characterized by the accumulation of deposits mainly localized to the cone-rich macular region of the eye. Dystrophy can be limited to the retina or be part of a syndrome. Unlike nonsyndromic cone-rod dystrophies, syndromic cone-rod dystrophies are genetically heterogeneous with mutations in genes encoding structural, cell-adhesion, and transporter proteins. Using a genome-wide single-nucleotide polymorphism (SNP) haplotype analysis to fine map the locus and a gene-candidate approach, we identified homozygous mutations in the ancient conserved domain protein 4 gene (CNNM4) that either generate a truncated protein or occur in highly conserved regions of the protein. Given that CNNM4 is implicated in metal ion transport, cone-rod dystrophy and amelogenesis imperfecta may originate from abnormal ion homeostasis.
Date of Publication
2009-02
Publication Type
Article
Subject(s)
Language(s)
en
Contributor(s)
Polok, Bozena | |
Ambresin, Aude | |
Chouery, Eliane | |
Bolay, Sylvain | |
Meunier, Isabelle | |
Nan, Francis | |
Hamel, Christian | |
Munier, Francis L | |
Thilo, Bernard | |
Mégarbané, André | |
Schorderet, Daniel F |
Additional Credits
Series
American journal of human genetics
Publisher
Cell Press
ISSN
0002-9297
Access(Rights)
restricted