Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia.

Two heterozygous mutations in NFATC1 in a patient with Tricuspid Atresia.

Tricuspid Atresia (TA) is a rare form of congenital heart disease (CHD) with usually poor prognosis in humans. It presents as a complete absence of the right atrio-ventricular connection secured normally by the tricuspid valve. Defects in the tricuspid valve are so far not associated with any geneti...

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Bibliographic Details
Main Authors: Zahi Abdul-Sater, Amin Yehya, Jean Beresian, Elie Salem, Amina Kamar, Serine Baydoun, Kamel Shibbani, Ayman Soubra, Fadi Bitar, Georges Nemer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3511479?pdf=render

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http://europepmc.org/articles/PMC3511479?pdf=render

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