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Missense mutation G296S in GATA4 is not responsible for cardiac septal defects

BACKGROUND: The most common type of congenital heart disease is the cardiac septal defects, which has reported to be caused by a missense mutation (G296S) in exon 3 of the GATA4 gene. AIMS: The present study was undertaken to find out whether GATA4 gene is the prime cause of the septal defects in My...

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Autores principales: Ramegowda, Smitha, Kumar, Arun, Savitha, Mysore R., Krishnamurthy, Balasundaram, Doddaiah, Narayanappa, Ramachandra, Nallur B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168151/
https://www.ncbi.nlm.nih.gov/pubmed/21957339
http://dx.doi.org/10.4103/0971-6866.32032
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author Ramegowda, Smitha
Kumar, Arun
Savitha, Mysore R.
Krishnamurthy, Balasundaram
Doddaiah, Narayanappa
Ramachandra, Nallur B.
author_facet Ramegowda, Smitha
Kumar, Arun
Savitha, Mysore R.
Krishnamurthy, Balasundaram
Doddaiah, Narayanappa
Ramachandra, Nallur B.
author_sort Ramegowda, Smitha
collection PubMed
description BACKGROUND: The most common type of congenital heart disease is the cardiac septal defects, which has reported to be caused by a missense mutation (G296S) in exon 3 of the GATA4 gene. AIMS: The present study was undertaken to find out whether GATA4 gene is the prime cause of the septal defects in Mysore population. MATERIALS AND METHODS: GATA4 gene analyses were undertaken on 21 confirmed CHD cases by PCR and DNA sequencing. RESULTS AND CONCLUSION: Analysis of this particular mutation in 21 septal defect patients revealed that none of the patients had the mutation, indicating that this mutation is population specific or septal defect in Mysore population is caused due to mutations in other regions of the GATA4 gene.
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spelling pubmed-31681512011-09-28 Missense mutation G296S in GATA4 is not responsible for cardiac septal defects Ramegowda, Smitha Kumar, Arun Savitha, Mysore R. Krishnamurthy, Balasundaram Doddaiah, Narayanappa Ramachandra, Nallur B. Indian J Hum Genet Short Communication BACKGROUND: The most common type of congenital heart disease is the cardiac septal defects, which has reported to be caused by a missense mutation (G296S) in exon 3 of the GATA4 gene. AIMS: The present study was undertaken to find out whether GATA4 gene is the prime cause of the septal defects in Mysore population. MATERIALS AND METHODS: GATA4 gene analyses were undertaken on 21 confirmed CHD cases by PCR and DNA sequencing. RESULTS AND CONCLUSION: Analysis of this particular mutation in 21 septal defect patients revealed that none of the patients had the mutation, indicating that this mutation is population specific or septal defect in Mysore population is caused due to mutations in other regions of the GATA4 gene. Medknow Publications 2007 /pmc/articles/PMC3168151/ /pubmed/21957339 http://dx.doi.org/10.4103/0971-6866.32032 Text en © Indian Journal of Human Genetics http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Ramegowda, Smitha
Kumar, Arun
Savitha, Mysore R.
Krishnamurthy, Balasundaram
Doddaiah, Narayanappa
Ramachandra, Nallur B.
Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
title Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
title_full Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
title_fullStr Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
title_full_unstemmed Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
title_short Missense mutation G296S in GATA4 is not responsible for cardiac septal defects
title_sort missense mutation g296s in gata4 is not responsible for cardiac septal defects
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168151/
https://www.ncbi.nlm.nih.gov/pubmed/21957339
http://dx.doi.org/10.4103/0971-6866.32032
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