Suscripción institucional·Artículo·2002·Inglés

Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations

Alvaro Blanch; Olga Roche; Eduardo López-Granados; Gumersindo Fontán; Margarita López-Trascasa

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Cómo citar

Alvaro Blanch, & Olga Roche, & Eduardo López-Granados, & Gumersindo Fontán, & Margarita López-Trascasa (2002). Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations. https://doi.org/10.1002/humu.9073