A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneys-Reference-Cited by-同舟云学术

A ZPR1 mutation is associated with a novel syndrome of growth restriction, distinct craniofacial features, alopecia, and hypoplastic kidneys

Published:2018-06-29 Issue:3-4 Volume:94 Page:303-312
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Ito Y.A.¹,Smith A.C.¹,Kernohan K.D.¹,Pena I.A.¹,Ahmed A.¹,McDonell L.M.¹,Beaulieu C.¹,Bulman D.E.¹,Smidt A.²³,Sawyer S.L.¹,Dyment D.A.¹^ORCID,Boycott K.M.¹^ORCID,Clericuzio C.L.²,

Affiliation:

1. Children's Hospital of Eastern Ontario Research Institute; University of Ottawa; Ottawa Canada

2. Division of Genetics/Dysmorphology, Department of Pediatrics; University of New Mexico School of Medicine; Albuquerque New Mexico

3. Department of Dermatology; University of New Mexico School of Medicine; Albuquerque New Mexico

Funder

Children's Hospital of Eastern Ontario Foundation

Génome Québec

Ontario Research Fund

Ontario Genomics Institute

Canadian Institutes of Health Research

Genome Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13388/fullpdf

Reference38 articles.

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