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The autosomal recessive mode of inheritance of C1 r deficiency in a large Puerto Rican family

All living members of three generations of a large family with C1 r deficiency were studied. The two index cases showed undetectable C1 r and partial deficiency of C1 s associated with cutaneous, renal and joint disease as described previously (Moncada et al., 1972). The quantitative C1 q, C1 r and...

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Detalhes bibliográficos
Main Authors: De Bracco, María M. E., Windhorst, Dorothy, Stroud, R. M., Moncada, B.
Formato: Artigo
Idioma:Inglês
Publicado em: 1974
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1553918/
https://ncbi.nlm.nih.gov/pubmed/4219876
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