A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A-Reference-Cited by-同舟云学术

A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A

Published:2019-02-27 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Demal Till Joscha,Heise Melina,Reiz Benedikt,Dogra Deepika,Brænne Ingrid,Reichenspurner Hermann,Männer Jörg,Aherrahrou Zouhair,Schunkert Heribert,Erdmann Jeanette,Abdelilah-Seyfried Salim

Funder

Joachim Herz Stiftung: "Add-on Fellowship for Interdisciplinary Sciences"

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-39648-7.pdf

Reference65 articles.

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2. Hoffman, J. I. Incidence of congenital heart disease: II. Prenatal incidence. Pediatr. Cardiol. 16, 155–165 (1995).

3. Wessels, M. W. & Willems, P. J. Genetic factors in non-syndromic congenital heart malformations. Clin. Genet. 78, 103–123 (2010).

4. Eisenberg, L. M. & Markwald, R. R. Molecular regulation of atrioventricular valvuloseptal morphogenesis. Circ. Res. 77, 1–6 (1995).

5. Calkoen, E. E. et al. Atrioventricular septal defect: From embryonic development to long-term follow-up. Int. J. Cardiol. 202, 784–795 (2016).

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