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Lack of association between osteoarthritis of the hip and gene polymorphisms of VDR, COL1A1, and COL2A1 in postmenopausal women

✍ Scribed by J. Aerssens; J. Dequeker; J. Peeters; S. Breemans; S. Boonen

Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
521 KB
Volume
41
Category
Article
ISSN
0004-3591

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πŸ“œ SIMILAR VOLUMES

Lack of correlation between the type of
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## Communicated by Peter Byers Osteogenesis imperfecta (OI) is caused by mutations in COL1A1 and COL1A2 that code for the a1 and a2 chains of type I collagen. Phenotypes correlate with the mutation types in that COL1A1 null mutations lead to OI type I, and structural mutations in a1(I) or a2(I) lea

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The original article to which this Erratum refers was published in Human Mutation 24: 147-154 (2004). In Table 1 of the published original article, the fourth mutation should be c.913G4C (not c.913G4A as originally printed) and it should be bolded as it is a novel mutation. In addition, the last mu