Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family. (2016)
Attributed to:
Identification of Major Risk Alleles for Schizophrenia in Consanguineous Families
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/ajmg.a.37690
PubMed Identifier: 27148795
Publication URI: http://europepmc.org/abstract/MED/27148795
Type: Journal Article/Review
Volume: 170
Parent Publication: American journal of medical genetics. Part A
Issue: 7
ISSN: 1552-4825