Familial thrombocytosis caused by the novel germ‐line mutation p.Pro106Leu in the MPL gene
Abstract
Familial thrombosis (FT) has been described as a rare autosomal-dominant disorder, mostly caused by activating mutations of the thrombopoietin gene (THPO). Other cases of FT have been linked to one of two different germline mutations in the myeloproliferative leukaemia virus oncogene gene (MPL), which codes for the thrombopoietin receptor MPL. We studied an Arab family with two siblings with severe thrombocytosis by linkage analysis and obtained...
Paper Details
Title
Familial thrombocytosis caused by the novel germ‐line mutation p.Pro106Leu in the MPL gene
Published Date
Dec 17, 2008
Volume
144
Issue
2
Pages
185 - 194
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