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