The dominant-negative von Willebrand factor gene deletion p.P1127_C1948delinsR: molecular mechanism and modulation.
about
Identification and functional analysis of a novel von Willebrand factor mutation in a family with type 2A von Willebrand disease.An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease.The molecular basis of von Willebrand disease: the under investigated, the unexpected and the overlooked.Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis/activity.Large deletions identified in patients with von Willebrand disease using multiple ligation-dependent probe amplification.
P2860
The dominant-negative von Willebrand factor gene deletion p.P1127_C1948delinsR: molecular mechanism and modulation.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
The dominant-negative von Will ...... ular mechanism and modulation.
@en
The dominant-negative von Will ...... ular mechanism and modulation.
@nl
type
label
The dominant-negative von Will ...... ular mechanism and modulation.
@en
The dominant-negative von Will ...... ular mechanism and modulation.
@nl
prefLabel
The dominant-negative von Will ...... ular mechanism and modulation.
@en
The dominant-negative von Will ...... ular mechanism and modulation.
@nl
P2093
P50
P1433
P1476
The dominant-negative von Will ...... ular mechanism and modulation.
@en
P2093
Alessandra Casonato
Caterina Casari
Francesco Bernardi
Stefano Lancellotti
P304
P356
10.1182/BLOOD-2010-02-268920
P407
P577
2010-08-27T00:00:00Z