Crossmark

Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease

Crossref DOI link: https://doi.org/10.1186/s12872-018-0867-4

Published Online: 2018-07-03

Published Print: 2018-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Razmara, Ehsan

Garshasbi, Masoud http://orcid.org/0000-0002-5508-7903
License Information

Text and Data Mining valid from 2018-07-03
More Information

Article History

Received: 19 February 2018

Accepted: 20 June 2018

First Online: 3 July 2018

Ethics approval and consent to participate

: The study protocol was approved by the local medical ethics committee of Tarbiat Modares University, Tehran, Iran. Informed written consents were obtained from all individuals. All of the patient’s clinical information and the medical histories were collected at the Department of Medical Genetics, DeNA Laboratory, Tehran, Iran. The parental consent was obtained for the patient who was under 16.

: Not applicable.

: The authors declare that they have no competing interests.

: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.