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Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the TBXAS1 gene.
No clinical trials have been registered for platelet-type bleeding disorder 14.
5 publications have been identified in PubMed for platelet-type bleeding disorder 14. Research spans Case Report / Case Series (40%), Epidemiology / Natural History (40%), and Review / Meta-Analysis (20%).
Ben Lamine Z (2026). [PMID: 41955421](https://pubmed.ncbi.nlm.nih.gov/41955421/). *Lab Med*. [Review / Meta-Analysis]
Sherief LM (2025). [PMID: 40301132](https://pubmed.ncbi.nlm.nih.gov/40301132/). *Eur J Pediatr*. [Epidemiology / Natural History]
Wong G (2025). [PMID: 39740654](https://pubmed.ncbi.nlm.nih.gov/39740654/). *Pediatr Neurosurg*. [Case Report / Case Series]
Kharat SV (2025). [PMID: 41100648](https://pubmed.ncbi.nlm.nih.gov/41100648/). *Indian J Med Res*. [Epidemiology / Natural History]
Şal O (2024). [PMID: 38926208](https://pubmed.ncbi.nlm.nih.gov/38926208/). *Surg Case Rep*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 6:43 AM UTC
Online Mendelian Inheritance in Man