Mutations in KPTN cause macrocephaly, neurodevelopmental delay, and seizures. (2014)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2013.10.001

PubMed Identifier: 24239382

Publication URI: http://europepmc.org/abstract/MED/24239382

Type: Journal Article/Review

Volume: 94

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297