A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome. (2018)

First Author: Roche EF

Attributed to: Enabling technologies funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/cen.13827

PubMed Identifier: 30086211

Publication URI: http://europepmc.org/abstract/MED/30086211

Type: Journal Article/Review

Volume: 89

Parent Publication: Clinical endocrinology

Issue: 6

ISSN: 0300-0664