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Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Stefan Gräf*, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen M. Treacy, Katherine Yates, Louise C. Daugherty, Olga Shamardina, Deborah Whitehorn, Simon Holden, Micheala Aldred, Harm J. Bogaard
*Corresponding author for this work
- Cambridge University Hospitals NHS Foundation Trust
- NIHR BioResource - Rare Diseases
- Departments of Molecular Genetics and Laboratory Medicine and Pathobiology
- Royal Papworth Hospital NHS Foundation Trust
- St George's, University of London
- Addenbrooke's Hospital
- Cleveland Clinic Foundation
- VU University Hospital
- Golden Jubilee National Hospital
- UCL University College London
- Histopathology Department, Royal Hallamshire Hospital, Sheffield, UK.
- Newcastle University Hospital
- University of Pavia
- IRCCS Foundation Policlinico San Matteo
- Paris 3
- Justus-Liebig University
- Imperial College London
- National Heart and Lung Institute
- INSERM
- Ludwig-Boltzmann Institute for Clinical Forensic Imaging
- Medizinische Universität
- Royal United Hospitals Bath NHS Foundation Trust
Research output: Contribution to journal › Article › peer-review
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