Structural analyses of the polymorphic area in type II collagen gene.
about
Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia.Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathyPCR detection of a HindIII polymorphism in the human gene for type II procollagen (COL2A1).Type II collagen mutations in rare and common cartilage diseases.Conservation of the sizes of 53 introns and over 100 intronic sequences for the binding of common transcription factors in the human and mouse genes for type II procollagen (COL2A1).
P2860
Structural analyses of the polymorphic area in type II collagen gene.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Structural analyses of the polymorphic area in type II collagen gene.
@en
type
label
Structural analyses of the polymorphic area in type II collagen gene.
@en
prefLabel
Structural analyses of the polymorphic area in type II collagen gene.
@en
P2860
P1433
P1476
Structural analyses of the polymorphic area in type II collagen gene.
@en
P2093
Peltonen L
P2860
P304
P356
10.1016/0014-5793(89)80713-6
P407
P577
1989-07-01T00:00:00Z