Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations.
about
Identification of missense mutations in exon 16 of factor VIII gene in mild and moderate cases with hemophilia A.In silico profiling of deleterious amino acid substitutions of potential pathological importance in haemophlia A and haemophlia B.Severe Hemophilia A in a Male Old English Sheep Dog with a C→T Transition that Created a Premature Stop Codon in Factor VIII.Mutation analysis in 51 patients with haemophilia A: report of 10 novel mutations and correlations between genotype and clinical phenotype.
P2860
Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Molecular pathology of haemoph ...... n of 36 independent mutations.
@en
Molecular pathology of haemoph ...... n of 36 independent mutations.
@nl
type
label
Molecular pathology of haemoph ...... n of 36 independent mutations.
@en
Molecular pathology of haemoph ...... n of 36 independent mutations.
@nl
prefLabel
Molecular pathology of haemoph ...... n of 36 independent mutations.
@en
Molecular pathology of haemoph ...... n of 36 independent mutations.
@nl
P2093
P2860
P1433
P1476
Molecular pathology of haemoph ...... n of 36 independent mutations.
@en
P2093
Caglayan SH
P2860
P304
P356
10.1046/J.1365-2516.2001.00548.X
P577
2001-09-01T00:00:00Z