Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families.

Belbézier, Aude; Hardy, Gaelle; Marlu, Raphael; Defendi, Federica; Dumestre Perard, Chantal; Boccon-Gibod, Isabelle; Launay, David; Bouillet, Laurence

Belbézier, Aude; Hardy, Gaelle; Marlu, Raphael; Defendi, Federica; Dumestre Perard, Chantal; Boccon-Gibod, Isabelle; Launay, David; Bouillet, Laurence.

Afiliação

Belbézier A; Department of Internal Medicine, Grenoble University Hospital, Grenoble, France.
Hardy G; National Reference Centre for Angioedema, CREAK, Grenoble, France.
Marlu R; Laboratory of Molecular Genetics, Department of Genetic Biology, Grenoble University Hospital, Grenoble, France.
Defendi F; National Reference Centre for Angioedema, CREAK, Grenoble, France.
Dumestre Perard C; Laboratory of Hemostasis, Grenoble University Hospital, Grenoble, France.
Boccon-Gibod I; National Reference Centre for Angioedema, CREAK, Grenoble, France.
Launay D; Laboratory of Immunology, Grenoble University Hospital, Grenoble, France.
Bouillet L; National Reference Centre for Angioedema, CREAK, Grenoble, France.

Allergy ; 73(11): 2237-2239, 2018 11.

Article em En | MEDLINE | ID: mdl-29952006

Assuntos

Angioedemas Hereditários; Proteína Inibidora do Complemento C1/genética; Humanos; Mutação; Plasminogênio

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Angioedemas Hereditários Limite: Humans Idioma: En Revista: Allergy Ano de publicação: 2018 Tipo de documento: Article

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