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  3. Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.
 

Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.

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BORIS DOI
10.7892/boris.101789
Publisher DOI
10.1016/j.ajhg.2009.01.006
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)
600 Technology > 610 Medicine & health
Language(s)
en
Contributor(s)
Polok, Bozena
Escher, Pascalorcid-logo
Universitätsklinik für Augenheilkunde
Ambresin, Aude
Chouery, Eliane
Bolay, Sylvain
Meunier, Isabelle
Nan, Francis
Hamel, Christian
Munier, Francis L
Thilo, Bernard
Mégarbané, André
Schorderet, Daniel F
Additional Credits
Universitätsklinik für Augenheilkunde
Series
American journal of human genetics
Publisher
Cell Press
ISSN
0002-9297
Access(Rights)
restricted
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