Glanzmann thrombasthenia: genetic basis and clinical correlates

Glanzmann thrombasthenia (GT) is an autosomal recessive disorder of platelet aggregation caused by quantitative or qualitative defects in integrins αIIb and β3. These integrins are encoded by the ITGA2B and ITGB3 genes and form platelet glycoprotein (GP)IIb/IIIa, which acts as the principal platelet...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Haematologica
मुख्य लेखकों: Botero, Juliana Perez, Lee, Kristy, Branchford, Brian R, Bray, Paul F, Freson, Kathleen, Lambert, Michele P., Luo, Minjie, Mohan, Shruthi, Ross, Justyne E., Bergmeier, Wolfgang, Di Paola, Jorge
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Ferrata Storti Foundation 2020
विषय:
Review Article
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC7109743/
https://ncbi.nlm.nih.gov/pubmed/32139434
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2018.214239
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