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  3. Identification and Functional Characterization of Genetic Variants Associated with Specific Clinical Phenotypes in Hereditary Angioedema due to C1 Inhibitor Deficiency: An Unbiased Approach.

Identification and Functional Characterization of Genetic Variants Associated with Specific Clinical Phenotypes in Hereditary Angioedema due to C1 Inhibitor Deficiency: An Unbiased Approach.

Datos básicos

Protocolo:
GENOMAEH_01
EUDRACT:
NCT:
Centro:
HOSPITAL UNIVERSITARI I POLITÈCNIC LA FE
Año de incio:
2023
Año de finalización:
PI BIOMÉDICA

Documentos

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Participantes

Grupos

Financiadores - Promotores

FUNDACIÓ HOSPITAL UNIVERSITARI VALL D’HEBRON - INSTITUT DE RECERCA

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