Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.
| Data(s) |
2011
|
|---|---|
| Resumo |
Using exome sequencing and a variant prioritization strategy that focuses on loss-of-function variants, we identified biallelic, loss-of-function CEP57 mutations as a cause of constitutional mosaic aneuploidies. CEP57 is a centrosomal protein and is involved in nucleating and stabilizing microtubules. Our findings indicate that these and/or additional functions of CEP57 are crucial for maintaining correct chromosomal number during cell division. |
| Identificador |
http://serval.unil.ch/?id=serval:BIB_7016C1743532 isbn:1546-1718 (Electronic) pmid:21552266 doi:10.1038/ng.822 isiid:000291017000008 |
| Idioma(s) |
en |
| Fonte |
Nature Genetics, vol. 43, no. 6, pp. 527-529 |
| Tipo |
info:eu-repo/semantics/article article |