GATA4 Specific Nonsynonymous Single-Nucleotide Polymorphisms in Congenital Heart Disease Patients of Mysore, India-Reference-Cited by-同舟云学术

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GATA4 Specific Nonsynonymous Single-Nucleotide Polymorphisms in Congenital Heart Disease Patients of Mysore, India

Published:2011-10 Issue:10 Volume:15 Page:715-720
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Dinesh Sosalagere M.¹,Lingaiah Kusuma¹,Savitha Mysore R.²,Krishnamurthy Balasundaram²,Narayanappa Doddaiah³,Ramachandra Nallur B.¹

Affiliation:

1. Genomics Laboratory, Department of Studies in Zoology, University of Mysore, Mysore, India.

2. Department of Pediatrics, Cheluvamba Hospital, Mysore Medical College, Mysore, India.

3. Department of Pediatrics, JSS Medical College and Hospital, Mysore, India

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2010.0278

Reference28 articles.

1. Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India

2. Insights into the genetic basis of congenital heart disease

3. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

4. Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects

5. Phenotypes withGATA4 orNKX2.5 mutations in familial atrial septal defect

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1. Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation;OMICS: A Journal of Integrative Biology;2024-07-01

2. Sequence variations in GATA4 and CITED2 gene among patients with cardiac septation defects from Xinjiang, China;Cardiology in the Young;2024-03-08

3. Case–control association study of congenital heart disease from a tertiary paediatric cardiac centre from North India;BMC Pediatrics;2023-06-15

4. In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease;Journal of Cardiovascular and Thoracic Research;2021-11-01

5. Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects;The Eurasian Journal of Medicine;2020-10-28

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