Glanzmann Thrombasthenia
What's New
Last Posted: Mar 10, 2023
- ITGA2B and ITGB3 gene mutations associated with Glanzmann thrombasthenia.
Nurden Alan T, et al. Platelets 2017 0 (1) 98-101 - [Diagnostic analysis of glanzmann thrombasthenia caused by two novel ITGA2B gene mutations].
Sun A X, et al. Zhonghua er ke za zhi = Chinese journal of pediatrics 2017 0 (9) 708-709 - High-throughput elucidation of thrombus formation reveals sources of platelet function variability.
van Geffen Johanna P, et al. Haematologica 2018 0 (6) 1256-1267 - From thrombasthenia to next generation thrombocytopenia: Neonatal alloimmune thrombocytopenia induced by maternal Glanzmann thrombasthenia.
Barg Assaf Arie, et al. Pediatric blood & cancer 2018 0 (12) e27376 - Prevalence of the Mutations Responsible for Glanzmann Thrombasthenia in Horses in Brazil.
Leite Raíssa O, et al. Animals : an open access journal from MDPI 2019 0 (11) - Molecular yield of targeted sequencing for Glanzmann thrombasthenia patients.
Owaidah Tarek, et al. NPJ genomic medicine 2019 0 4 - Association of autosomal-recessive-type distal renal tubular acidosis and Glanzmann thrombasthenia as a consequence of runs of homozygosity.
Aso Keiko, et al. Clinical case reports 2022 0 (7) e6070 - Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.
Ross Justyne E et al. Blood advances 2021 Jan 5(2) 414-431 - Study of the Relationship between HPA-1 and HPA-5 Gene Polymorphisms and Refractory to Platelet Therapy and Recombinant Factor VII in Glanzmann Thrombasthenia Patients in Southeast of Iran.
Naderi Majid, et al. International journal of hematology-oncology and stem cell research 2018 1 (1) 43-48 - Clinical utility gene card for: Glanzmann thrombasthenia.
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- Page last reviewed:Feb 1, 2024
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