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Parsing the repertoire of GPIb-IX-V disorders
In this issue of Blood, Sivapalaratnam et al(1) report an association between unique, rare monoallelic variants in GP1BB, which encodes the glycoprotein (GP)Ibβ subunit of the platelet GPIb-IX-V complex, and autosomal dominant macrothrombocytopenia.
Guardat en:
| Publicat a: | Blood |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society of Hematology
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5270391/ https://ncbi.nlm.nih.gov/pubmed/28126957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2016-12-753186 |
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