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Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.

Authors :
Snape K
Hanks S
Ruark E
Barros-Núñez P
Elliott A
Murray A
Lane AH
Shannon N
Callier P
Chitayat D
Clayton-Smith J
Fitzpatrick DR
Gisselsson D
Jacquemont S
Asakura-Hay K
Micale MA
Tolmie J
Turnpenny PD
Wright M
Douglas J
Rahman N
Source :
Nature genetics [Nat Genet] 2011 Jun; Vol. 43 (6), pp. 527-9. Date of Electronic Publication: 2011 May 08.
Publication Year :
2011

Abstract

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.

Details

Language :
English
ISSN :
1546-1718
Volume :
43
Issue :
6
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
21552266
Full Text :
https://doi.org/10.1038/ng.822