Familial thrombocytosis caused by the novel germ‐line mutation p.Pro106Leu in the MPL gene
Summary 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 (M...
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Veröffentlicht in: | British journal of haematology 2009-01, Vol.144 (2), p.185-194 |
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Sprache: | eng |
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