Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A.
about
Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations.Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.Detection of new mutations and molecular pathology of mild and moderate haemophilia A patients from southern Brazil.Spectrum of Molecular Defects in 216 Chinese Families With Hemophilia A: Identification of Noninversion Mutation Hot Spots and 42 Novel Mutations.Molecular diagnosis of haemophilia A in patients from Senegal.Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A.
P2860
Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Computational and molecular ap ...... n patients with haemophilia A.
@en
Computational and molecular ap ...... n patients with haemophilia A.
@nl
type
label
Computational and molecular ap ...... n patients with haemophilia A.
@en
Computational and molecular ap ...... n patients with haemophilia A.
@nl
prefLabel
Computational and molecular ap ...... n patients with haemophilia A.
@en
Computational and molecular ap ...... n patients with haemophilia A.
@nl
P2093
P2860
P1433
P1476
Computational and molecular ap ...... n patients with haemophilia A.
@en
P2093
P2860
P304
P356
10.1111/J.1365-2516.2011.02640.X
P577
2011-08-26T00:00:00Z