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A 13-bp deletion in α(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder caused by lack or dysfunction of α(IIb)β(3) in platelets. GT is relatively frequent in highly inbred populations. We previously identified a 13-bp deletion in the α(IIb) gene that causes in-frame deletion of six amino acid...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2005
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1557653/ https://ncbi.nlm.nih.gov/pubmed/16359514 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1538-7836.2005.01618.x |
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