GATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation-Reference-Cited by-同舟云学术

GATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation

Published:2010-12 Issue:6 Volume:14 Page:797-802
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Butler Tanya L.¹²,Esposito Giorgia¹,Blue Gillian M.¹,Cole Andrew D.¹,Costa Mauro W.³,Waddell Leigh B.¹,Walizada Gina¹,Sholler Gary F.¹²,Kirk Edwin P.⁴,Feneley Michael³⁵,Harvey Richard P.³⁶,Winlaw David S.¹²

Affiliation:

1. Heart Centre for Children, The Children's Hospital at Westmead, Westmead, Australia.

2. Sydney Medical School, University of Sydney, Sydney, Australia.

3. Victor Chang Cardiac Research Institute, Darlinghurst, Australia.

4. Sydney Children's Hospital, Randwick, Australia.

5. St. Vincent's Hospital, Darlinghurst, Australia.

6. Faculties of Science and Medicine, University of New South Wales, Kensington, Australia.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2010.0028

Reference30 articles.

1. 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families

2. Listening to silence and understanding nonsense: exonic mutations that affect splicing

3. ESEfinder: a web resource to identify exonic splicing enhancers

4. Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors

5. Activation of the Calcineurin/NFAT Signalling Cascade Starts Early in Human Hypertrophic Myocardium

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