Osteogenesis imperfecta mutations may probe vital functional domains (e.g. proteoglycan binding sites) of type 1 collagen fibrils. | Cell Biochem Funct;15(4): 283-6, 1997 Dec. | MEDLINE

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Osteogenesis imperfecta mutations may probe vital functional domains (e.g. proteoglycan binding sites) of type 1 collagen fibrils.

Scott, J E; Tenni, R.

Affiliation

Scott JE; Department of Chemical Morphology, Manchester University, UK.

Cell Biochem Funct ; 15(4): 283-6, 1997 Dec.

Article in En | MEDLINE | ID: mdl-9415975

Subject(s)

Collagen/chemistry; Collagen/genetics; Osteogenesis Imperfecta/genetics; Point Mutation; Proteoglycans/metabolism; Binding Sites; Collagen/metabolism; Humans

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Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis Imperfecta / Proteoglycans / Collagen / Point Mutation Limits: Humans Language: En Journal: Cell Biochem Funct Year: 1997 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom

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Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis Imperfecta / Proteoglycans / Collagen / Point Mutation Limits: Humans Language: En Journal: Cell Biochem Funct Year: 1997 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom