Identification of a novel and recurrent mutation in the SERPING1 gene in patients with hereditary angioedema.
about
Recombinant replacement therapy for hereditary angioedema due to C1 inhibitor deficiencyA Nationwide Study of Norwegian Patients with Hereditary Angioedema with C1 Inhibitor Deficiency Identified Six Novel Mutations in SERPING1.Impaired Endothelial Function in Hereditary Angioedema During the Symptom-Free Period.
P2860
Identification of a novel and recurrent mutation in the SERPING1 gene in patients with hereditary angioedema.
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
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2013年學術文章
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name
Identification of a novel and ...... ts with hereditary angioedema.
@en
Identification of a novel and ...... ts with hereditary angioedema.
@nl
type
label
Identification of a novel and ...... ts with hereditary angioedema.
@en
Identification of a novel and ...... ts with hereditary angioedema.
@nl
prefLabel
Identification of a novel and ...... ts with hereditary angioedema.
@en
Identification of a novel and ...... ts with hereditary angioedema.
@nl
P2093
P50
P1433
P1476
Identification of a novel and ...... nts with hereditary angioedema
@en
P2093
Carmela Zizzo
Gavino Piseddu
Luisa Fenu
Maria P Barca
Paolo Emilio Manconi
P304
P356
10.1016/J.CLIM.2013.03.007
P577
2013-03-27T00:00:00Z