TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons. (2016)

First Author: Caubit X
Attributed to:  Molecular bases of congenital bladder disease: the urofacial syndome (UFS) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.3681

PubMed Identifier: 27668656

Publication URI: http://europepmc.org/abstract/MED/27668656

Type: Journal Article/Review

Volume: 48

Parent Publication: Nature genetics

Issue: 11

ISSN: 1061-4036