Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.


Autoria(s): Snape K.; Hanks S.; Ruark E.; Barros-Núñez P.; Elliott A.; Murray A.; Lane A.H.; Shannon N.; Callier P.; Chitayat D.; Clayton-Smith J.; Fitzpatrick D.R.; Gisselsson D.; Jacquemont S.; Asakura-Hay K.; Micale M.A.; Tolmie J.; Turnpenny P.D.; Wright M.; Douglas J.; Rahman N.
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