Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome-Reference-Cited by-同舟云学术

Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome

Published:2010-06-02 Issue:1 Volume:88 Page:130-139
ISSN:0008-6363
Container-title:Cardiovascular Research
language:en
Short-container-title:Cardiovascular Research

Author:

Boogerd C. J. J.,Dooijes D.,Ilgun A.,Mathijssen I. B.,Hordijk R.,van de Laar I. M. B. H.,Rump P.,Veenstra-Knol H. E.,Moorman A. F. M.,Barnett P.,Postma A. V.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Link

http://academic.oup.com/cardiovascres/article-pdf/88/1/130/821941/cvq178.pdf

Reference44 articles.

1. FAMILIAL HEART DISEASE WITH SKELETAL MALFORMATIONS

2. The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome)

3. Chamber-Specific Cardiac Expression of Tbx5 and Heart Defects in Holt–Oram Syndrome

4. A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

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