Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. (2011)

First Author: Albers CA
Attributed to:  Statistical bioinformatics and genetics funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.885

PubMed Identifier: 21765411

Publication URI: http://europepmc.org/abstract/MED/21765411

Type: Journal Article/Review

Volume: 43

Parent Publication: Nature genetics

Issue: 8

ISSN: 1061-4036