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

Ehsan Razmara, Masoud Garshasbi

Open source

DOI: 10.1186/s12872-018-0867-4
Published: 2018-07-03
Container: BMC Cardiovascular Disorders
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1186/s12872-018-0867-4,
  title = {Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease},
  author = {Ehsan Razmara and Masoud Garshasbi},
  year = {2018},
  journal = {BMC Cardiovascular Disorders},
  doi = {10.1186/s12872-018-0867-4},
  url = {https://doi.org/10.1186/s12872-018-0867-4}
}

RIS

TY  - JOUR
TI  - Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease
AU  - Ehsan Razmara
AU  - Masoud Garshasbi
PY  - 2018
JO  - BMC Cardiovascular Disorders
DO  - 10.1186/s12872-018-0867-4
UR  - https://doi.org/10.1186/s12872-018-0867-4
ER  -

APA

Razmara, E., & Garshasbi, M. (2018). Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease. BMC Cardiovascular Disorders. https://doi.org/10.1186/s12872-018-0867-4

Source records

crossref · retrieved 2026-11-10T12:34:53.017Z