Nonrandom association of a type II procollagen genotype with achondroplasia.
Achondroplasia is an autosomal dominant disorder that involves defective endochondral bone formation. Type II collagen is the predominant collagen of cartilage. We found a HindIII polymorphic site in the normal Caucasian population by using the type II procollagen gene probe pgHCol(II)A. The presenc...
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| Yayımlandı: | Proc Natl Acad Sci U S A |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
1985
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC391143/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2991928/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.82.16.5465 |
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