Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.

Détails

Ressource 1Télécharger: 21552266_BIB_7016C1743532.pdf (488.15 [Ko])
Etat: Public
Version: Author's accepted manuscript
Licence: Non spécifiée
ID Serval
serval:BIB_7016C1743532
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.
Périodique
Nature Genetics
Auteur⸱e⸱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.
ISSN
1546-1718 (Electronic)
ISSN-L
1061-4036
Statut éditorial
Publié
Date de publication
2011
Volume
43
Numéro
6
Pages
527-529
Langue
anglais
Résumé
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.
Pubmed
Web of science
Création de la notice
14/06/2011 14:03
Dernière modification de la notice
30/04/2021 7:11
Données d'usage