In:
Clinical Case Reports, Wiley, Vol. 6, No. 6 ( 2018-06), p. 1109-1111
Abstract:
Congenital erythrocytosis is a hereditary disorder due to an increase in red cell mass that can be caused by mutations in proteins involved in HIF‐α pathway, as PHD2. Hereby, we describe a new familial mutation in PHD2 gene. Considering an increased thrombotic potential, patients began antiplatelet aggregation therapy and phlebotomies.
Type of Medium:
Online Resource
ISSN:
2050-0904
,
2050-0904
DOI:
10.1002/ccr3.2018.6.issue-6
Language:
English
Publisher:
Wiley
Publication Date:
2018
detail.hit.zdb_id:
2740234-4
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