Defects of type I procollagen metabolism correlated with decrease of prolidase activity in a case of lethal osteogenesis imperfecta

Author:

Galicka Anna,Wolczyñski Slawomir,Anchim Tomasz,Surazyñski Arkadiusz,Lesniewicz Ryszard,Palka Jerzy

Publisher

Wiley

Subject

Biochemistry

Reference44 articles.

1. Heritable diseases of collagen;Prockop;N. Engl. J. Med.,1984

2. Collagen genes and inherited connective tissue diseases;Cheah;Biochem. J.,1985

3. Genetic heterogeneity in osteogenesis imperfecta;Sillence;J. Med. Genet.,1979

4. Nuclear retention of Col1A1 messenger RNA identifies null alleles causing mild osteogenesis imperfecta;Redford-Badwal;J. Clin. Invest.,1996

5. Premature chain termination is a unifying mechanism for COL1A1 null alleles in osteogenesis imperfecta type I cell strains;Willing;Am. J. Hum. Genet.,1996

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