Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion.
about
Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
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2013年學術文章
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2013年學術文章
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name
Characterisation of the p.A146 ...... defective α-granule secretion.
@en
Characterisation of the p.A146 ...... defective α-granule secretion.
@nl
type
label
Characterisation of the p.A146 ...... defective α-granule secretion.
@en
Characterisation of the p.A146 ...... defective α-granule secretion.
@nl
prefLabel
Characterisation of the p.A146 ...... defective α-granule secretion.
@en
Characterisation of the p.A146 ...... defective α-granule secretion.
@nl
P2093
P50
P356
P1476
Characterisation of the p.A146 ...... defective α-granule secretion.
@en
P2093
Brigitte Spath
Carsten Bokemeyer
Florian Langer
James G White
Katharina Holstein
Tobias Obser
Ulrich Budde
P304
P356
10.1160/TH13-06-0462
P577
2013-12-12T00:00:00Z