Noncompaction cardiomyopathy in an infant with Walker-Warburg syndrome-Reference-Cited by-同舟云学术

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Noncompaction cardiomyopathy in an infant with Walker-Warburg syndrome

Published:2017-10-05 Issue:11 Volume:173 Page:3082-3086
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Abdullah Sarah¹,Hawkins Cynthia²,Wilson Gregory²,Yoon Grace³,Mertens Luc⁴,Carter Melissa T.⁵,Guerin Andrea¹³^ORCID

Affiliation:

1. Division of Medical Genetics; Department of Pediatrics; Kingston General Hospital; Queen's University; Kingston Canada

2. Division of Pathology; Department of Pediatric Laboratory Medicine; The Hospital for Sick Children; Toronto Canada

3. Division of Clinical and Metabolic Genetics; Department of Pediatrics; The Hospital for Sick Children; University of Toronto; Toronto Canada

4. Division of Cardiology; The Hospital for Sick Children; University of Toronto; Toronto Canada

5. Regional Genetics Program; The Children's Hospital of Eastern Ontario; Ottawa Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference13 articles.

1. Diagnostic criteria for Walker-Warburg syndrome;Dobyns;American Journal of Medical Genetics,1989

2. Cardiac findings in congenital muscular dystrophies;Finsterer;Pediatrics,2010

3. Walker-Warburg syndrome: Neurologic features and muscle membrane structure;Kanoff;Pediatric Neurology,1998

4. Walker-Warburg syndrome: Rare congenital muscular dystrophy associated with brain and eye abnormalities;Lee;Hong Kong Medical Journal,2014

5. Exome sequencing and functional validation in zebrafish identify gtdc2 mutations as a cause of Walker-Warburg syndrome;Manzini;The American Journal of Human Genetics,2012

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