Genetic screening of Congenital Short Bowel Syndrome patients confirms CLMP as the major gene involved in the recessive form of this disorder (2016)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ejhg.2016.58

PubMed Identifier: 27352967

Publication URI: http://europepmc.org/abstract/MED/27352967

Type: Journal Article/Review

Parent Publication: European Journal of Human Genetics

Issue: 11

ISSN: 1018-4813