A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3
about
von Willebrand disease: clinical and laboratory lessons learned from the large von Willebrand disease studiesAnoctamins.Assessment of the olfactory function in Italian patients with type 3 von Willebrand disease caused by a homozygous 253 Kb deletion involving VWF and TMEM16B/ANO2Management of inherited von Willebrand disease in 2007.von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein.Current management of patients with severe von Willebrand disease type 3: a 2012 update.Molecular, biophysical, and pharmacological properties of calcium-activated chloride channels.Phenotypic and genotypic characterization of 10 Finnish patients with von Willebrand disease type 3: discovery of two main mutations.Large deletions identified in patients with von Willebrand disease using multiple ligation-dependent probe amplification.
P2860
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P2860
A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3
description
im April 2007 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована у квітні 2007
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name
A common 253-kb deletion invol ...... von Willebrand disease type 3
@en
A common 253-kb deletion invol ...... von Willebrand disease type 3
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type
label
A common 253-kb deletion invol ...... von Willebrand disease type 3
@en
A common 253-kb deletion invol ...... von Willebrand disease type 3
@nl
prefLabel
A common 253-kb deletion invol ...... von Willebrand disease type 3
@en
A common 253-kb deletion invol ...... von Willebrand disease type 3
@nl
P2093
P2860
P1476
A common 253-kb deletion invol ...... von Willebrand disease type 3
@en
P2093
A. B. FEDERICI
G. CASTAMAN
J. OLDENBURG
R. MARSCHALEK
R. SCHNEPPENHEIM
P2860
P304
P356
10.1111/J.1538-7836.2007.02460.X
P577
2007-04-01T00:00:00Z