Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease

Abstract Background Pulmonary arterial hypertension (PAH) is a rare disease characterized by distinctive changes in pulmonary arterioles that lead to progressive pulmonary arterial pressures, right-sided heart failure, and a high mortality rate. Up to 30% of adult and 75% of pediatric PAH cases are...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Na Zhu, Carrie L. Welch, Jiayao Wang, Philip M. Allen, Claudia Gonzaga-Jauregui, Lijiang Ma, Alejandra K. King, Usha Krishnan, Erika B. Rosenzweig, D. Dunbar Ivy, Eric D. Austin, Rizwan Hamid, Michael W. Pauciulo, Katie A. Lutz, William C. Nichols, Jeffrey G. Reid, John D. Overton, Aris Baras, Frederick E. Dewey, Yufeng Shen, Wendy K. Chung
Format: Artigo
Langue:Inglês
Publié: BMC 2018-07-01
Collection:Genome Medicine
Sujets:
Pulmonary hypertension
Congenital heart disease
Exome sequencing
Genetic association study
Accès en ligne:http://link.springer.com/article/10.1186/s13073-018-0566-x
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires