Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families
about
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.Phenotype-genotype correlation in eight Polish patients with inherited Factor XIII deficiency: identification of three novel mutations.Congenital deficiency of factor XIII caused by two missense mutations in a Dutch family.
P2860
Seven novel mutations in the factor XIII A-subunit gene causing hereditary factor XIII deficiency in 10 unrelated families
description
article
@en
im Oktober 2004 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в жовтні 2004
@uk
name
Seven novel mutations in the f ...... iency in 10 unrelated families
@en
Seven novel mutations in the f ...... iency in 10 unrelated families
@nl
type
label
Seven novel mutations in the f ...... iency in 10 unrelated families
@en
Seven novel mutations in the f ...... iency in 10 unrelated families
@nl
prefLabel
Seven novel mutations in the f ...... iency in 10 unrelated families
@en
Seven novel mutations in the f ...... iency in 10 unrelated families
@nl
P2093
P2860
P1476
Seven novel mutations in the f ...... iency in 10 unrelated families
@en
P2093
A. Vysokovsky
A. Zivelin
N. Rosenberg
R. Eskaraev
U. Seligsohn
P2860
P304
P356
10.1111/J.1538-7836.2004.00908.X
P577
2004-10-01T00:00:00Z