A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation

scientific article published on 01 December 2010

A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.JACI.2010.07.037
P698PubMed publication ID20864152

P50authorMargarita López-TrascasaQ54422019
Christian DrouetQ57082941
P2093author name stringAlberto López-Lera
Sofía Garrido
Bertrand Favier
Rocío Mena de la Cruz
P433issue6
P921main subjecthomozygosityQ114049690
P304page(s)1307-10.e3
P577publication date2010-12-01
P1433published inThe Journal of Allergy and Clinical ImmunologyQ7743550
P1476titleA new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation
P478volume126

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Q41072058Fatal laryngeal angioedema: a case report and a workup of angioedema in a forensic setting
Q38818135Genetics of Hereditary Angioedema Revisited
Q64107494Identification and Mapping of a 2,009-bp DNA Deletion in of a Hereditary Angioedema Patient
Q48223638Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight
Q38025607Long-term prophylaxis in hereditary angio-oedema: a systematic review.
Q62273446Pathophysiology of Hereditary Angioedema
Q34805433Pediatric hereditary angioedema
Q90090895SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes

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