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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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Eng, C E, Pauli, R M, Strom, C M
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1985
Matèries:	Research Article
Accés en línia:	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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