PubMed:23317772 JSONTXT

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{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/23317772","sourcedb":"PubMed","sourceid":"23317772","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/23317772","text":"Recessive oligodontia linked to a homozygous loss-of-function mutation in the SMOC2 gene.\nOBJECTIVE: Recently, several genes have been reported with mutations or variants that underlie a number of syndromic and non-syndromic forms of oligodontia including MSX1, PAX9, AXIN2, EDA and WNT10A. This study aimed to identify the causal mutations in a consanguineous Pakistan family with oligodontia and microdontia.\nDESIGN: Exome sequencing was performed in two of affected members of the Pakistan family.\nRESULTS: The exome sequencing data revealed that the affected individuals were homozygous with a novel mutation in exon 8 of the SMOC2 gene, c.681T\u003eA (p.C227X).\nCONCLUSIONS: This is the second report describing SMOC2 mutations with oligodontia and microdontia underlining the key role for this signalling molecule in tooth 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