The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans

Minna Ampuja, Sabina Ericsson, Ilkka Paatero, Iftekhar Chowdhury, Jenna Villman, Martin Broberg, Amanda Ramste, Diego Balboa, Tiina Ojala, Jessica X. Chong, Michael J. Bamshad, James R. Priest, Markku Varjosalo, Riikka Kivelä, Emmi Helle

Open source

DOI
10.1016/j.xhgg.2025.100446
Published
2025-07
Container
Human Genetics and Genomics Advances
Publisher
Elsevier BV
Open access
unknown

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BibTeX

@article{allodium:10.1016/j.xhgg.2025.100446,
  title = {The ERBB2 c.1795C\>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans},
  author = {Minna Ampuja and Sabina Ericsson and Ilkka Paatero and Iftekhar Chowdhury and Jenna Villman and Martin Broberg and Amanda Ramste and Diego Balboa and Tiina Ojala and Jessica X. Chong and Michael J. Bamshad and James R. Priest and Markku Varjosalo and Riikka Kivelä and Emmi Helle},
  year = {2025},
  journal = {Human Genetics and Genomics Advances},
  doi = {10.1016/j.xhgg.2025.100446},
  url = {https://doi.org/10.1016/j.xhgg.2025.100446}
}

RIS

TY  - JOUR
TI  - The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans
AU  - Minna Ampuja
AU  - Sabina Ericsson
AU  - Ilkka Paatero
AU  - Iftekhar Chowdhury
AU  - Jenna Villman
AU  - Martin Broberg
AU  - Amanda Ramste
AU  - Diego Balboa
AU  - Tiina Ojala
AU  - Jessica X. Chong
AU  - Michael J. Bamshad
AU  - James R. Priest
AU  - Markku Varjosalo
AU  - Riikka Kivelä
AU  - Emmi Helle
PY  - 2025
JO  - Human Genetics and Genomics Advances
DO  - 10.1016/j.xhgg.2025.100446
UR  - https://doi.org/10.1016/j.xhgg.2025.100446
ER  - 

APA

Ampuja, M., Ericsson, S., Paatero, I., Chowdhury, I., Villman, J., Broberg, M., Ramste, A., Balboa, D., Ojala, T., Chong, J. X., Bamshad, M. J., Priest, J. R., Varjosalo, M., Kivelä, R., & Helle, E. (2025). The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans. Human Genetics and Genomics Advances. https://doi.org/10.1016/j.xhgg.2025.100446

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