Phenotypic Heterogeneity in the Gray Platelet Syndrome Extends to the Expression of TREM Family Member, TLT-1

The Gray platelet syndrome (GPS) is a rare inherited disorder linked to undefined molecular abnormalities that prevent the formation and maturation of α-granules. Here, we report studies on two patients from unrelated families that confirm phenotypic heterogeneity in the disease. First we used immun...

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Главные авторы: Nurden, Alan T., Nurden, Paquita, Bermejo, Emilsé, Combrié, Robert, McVicar, Daniel W., Washington, A. Valance
Формат: Artigo
Язык:Inglês
Опубликовано: 2008
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2694056/
https://ncbi.nlm.nih.gov/pubmed/18612537
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1160/TH08-02-0067
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