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Nat Genet. 2011 Mar 6;43(4):306-8. doi: 10.1038/ng.778.

Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis.

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  • 1CHU Nantes, Service de Génétique Médicale, Nantes, France.

Abstract

Hajdu-Cheney syndrome is a rare autosomal dominant skeletal disorder with facial anomalies, osteoporosis and acro-osteolysis. We sequenced the exomes of six unrelated individuals with this syndrome and identified heterozygous nonsense and frameshift mutations in NOTCH2 in five of them. All mutations cluster to the last coding exon of the gene, suggesting that the mutant mRNA products escape nonsense-mediated decay and that the resulting truncated NOTCH2 proteins act in a gain-of-function manner.

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PMID:
21378989
[PubMed - indexed for MEDLINE]
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