Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy. (2017)

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2017.01.019

PubMed Identifier: 28190459

Publication URI: http://europepmc.org/abstract/MED/28190459

Type: Journal Article/Review

Volume: 100

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297