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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...
Kaydedildi:
| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
1974
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1553918/ https://ncbi.nlm.nih.gov/pubmed/4219876 |
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