Data for Bernabeu-Herrero et al, Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT
<p>This dataset is for the 2024 manuscript<strong>: </strong></p> <p><strong>Bernabéu-Herrero ME, Patel D, Bielowka A, Zhu J, Jain K, Mackay IS, Chaves Guerrero P, Emanuelli G, Jovine L, Noseda M, Marciniak SJ, Aldred MA, Shovlin CL. </strong></p> <p><strong>Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT. </strong></p> <p><strong>Blood. 2024 May 30;143(22):2314-2331. </strong></p> <p><strong>doi: 10.1182/blood.2023021777. PMID: 38457357; PMCID: PMC11181359.</strong></p> <p>It was originally uploaded in 2021 ahead of an earlier manuscript submission<br>- see https://www.biorxiv.org/content/10.1101/2021.12.05.471269v1</p>
ShareScore
36/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 4
- Access
- 20
- Reuse readiness
- 8
- Engagement
- 0