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Article

Normal activated partial thromboplastin time in Chinese patients with mild hemophilia B.

Hematology (Amsterdam, Netherlands) - 1 Dec 2020

Wang Xiong, Tang Ning, Shen Na, Zhu Yaowu, Lu Yanjun, Gao Linna

Abstract excerpt

OBJECTIVES: Hemophilia B (HB, OMIM: 300746) is one of the most common bleeding disorders with an X-linked recessive inheritance pattern, caused by the deficiency of coagulation factor IX (FIX). FIX is encoded by the F9 gene located on Xq27.1. Diagnosis of HB is primarily suspected by prolonged activated partial thromboplastin time (APTT), decreased FIX activity (FIX:C) or genetic test of the F9 gene. We herein...

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Identifiers

PMID: 33295842
DOI: 10.1080/16078454.2020.1853403

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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