Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities-Reference-Cited by-同舟云学术

Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities

Published:2017-08-24 Issue:22 Volume:26 Page:4315-4326
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Giri Dinesh¹²,Vignola Maria Lillina³,Gualtieri Angelica³,Scagliotti Valeria³,McNamara Paul²,Peak Matthew⁴,Didi Mohammed¹,Gaston-Massuet Carles³,Senniappan Senthil¹²

Affiliation:

1. Department of Paediatric Endocrinology, Alder Hey Children’s Hospital NHS Foundation Trust, Liverpool, UK

2. Department of Women and Children's Health, Institute in the Park, University of Liverpool, Liverpool L12 2AP, UK

3. Centre for Endocrinology, William Harvey Research Institute, Barts & the London School of Medicine, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK

4. NIHR Alder Hey Clinical Research Facility for Experimental Medicine, Alder Hey Children's NHS Foundation Trust, Liverpool, L12 2AP, UK

Funder

MRC

Action Medical Research

University of Liverpool

CRF

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/22/4315/24339230/ddx318.pdf