Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
about
Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase geneCarrier detection through the use of abnormal deletion junction fragments in a case of haemophilia B involving complete deletion of the factor IX gene.Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B.Disappearance of inhibitor to factor IX in a patient with severe haemophilia B and immunological characterization of the inhibitor.Hemophilia B in a 46,XX female probably caused by non-random X inactivation.
P2860
Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
@en
type
label
Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
@en
prefLabel
Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
@en
P2093
P2860
P921
P356
P1476
Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.
@en
P2093
P2860
P304
P356
10.1172/JCI112880
P407
P577
1987-03-01T00:00:00Z