Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome: A biallelic deletion variant in DCAF17 , causing familial WSS

Saved in:
Bibliographic Details
Published in:Clinical genetics 2016-09, Vol.90 (3), p.263-269
Main Authors: Ali, R.H., Shah, K., Nasir, A., Steyaert, W., Coucke, P.J., Ahmad, W.
Format: Article
Language:English
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0009-9163
DOI:10.1111/cge.12700