Hemophilia B: molecular pathogenesis and mutation analysis.
about
Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach.Treatment and Prevention of Bleeds in Haemophilia Patients with Inhibitors to Factor VIII/IXCoagulation Factor IX (Recombinant), Albumin Fusion Protein (Albutrepenonacog Alfa; Idelvion®): A Review of Its Use in Haemophilia B.Diagnosis and phenotypic assessment of Pakistani Haemophilia B carriers.The first case report of a patient with coexisting hemophilia B and Down syndrome.Recurrent episodes of anaphylaxis in a patient with haemophilia B: a case report.First case report of hemophilia B Leyden in Japan.Multiplex ligation-dependent probe amplification as first mutation screening for large deletions and duplications in haemophilia.How I manage patients with inherited haemophilia A and B and factor inhibitors.Diagnosis and care of patients with mild haemophilia: practical recommendations for clinical management.Autologous and Heterologous Cell Therapy for Hemophilia B toward Functional Restoration of Factor IX.
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P2860
Hemophilia B: molecular pathogenesis and mutation analysis.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Hemophilia B: molecular pathogenesis and mutation analysis.
@ast
Hemophilia B: molecular pathogenesis and mutation analysis.
@en
type
label
Hemophilia B: molecular pathogenesis and mutation analysis.
@ast
Hemophilia B: molecular pathogenesis and mutation analysis.
@en
prefLabel
Hemophilia B: molecular pathogenesis and mutation analysis.
@ast
Hemophilia B: molecular pathogenesis and mutation analysis.
@en
P2860
P921
P356
P1476
Hemophilia B: molecular pathogenesis and mutation analysis
@en
P2093
A C Goodeve
P2860
P304
P356
10.1111/JTH.12958
P5008
P577
2015-05-18T00:00:00Z