R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.

R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.

AIMS: Heterozygous mutations in the transcription factor Nkx2.5 indicate a genetic cause for congenital heart diseases (CHDs) in human beings. The present study aimed to assess the prevalence of NKX2.5 mutations in Italian patients with sporadic non-syndromic and syndromic CHD, as well as to apprais...

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Bibliographic Details
Main Authors: Beffagna, G, Cecchetto, A, Dal Bianco, L, Lorenzon, A, Angelini, A, Padalino, M, Vida, V, Bhattacharya, S, Stellin, G, Rampazzo, A, Daliento, L
Format: Journal article
Language:English
Published: 2013

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