Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital.
- DOI
- 10.1080/03009734.2018.1483452
- Published
- 2018 Sep
- Container
- Upsala journal of medical sciences
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1080/03009734.2018.1483452,
title = {Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital.},
author = {Karlsson T and Cherif H},
year = {2018},
journal = {Upsala journal of medical sciences},
doi = {10.1080/03009734.2018.1483452},
url = {https://doi.org/10.1080/03009734.2018.1483452}
}RIS
TY - JOUR TI - Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital. AU - Karlsson T AU - Cherif H PY - 2018 JO - Upsala journal of medical sciences DO - 10.1080/03009734.2018.1483452 UR - https://doi.org/10.1080/03009734.2018.1483452 ER -
APA
T, K., & H, C. (2018). Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital.. Upsala journal of medical sciences. https://doi.org/10.1080/03009734.2018.1483452
Source records
- pubmed · retrieved 2026-09-25T10:59:24.003Z