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October 1, 1980Proceedings of the National Academy of SciencesOpen Access

A defect in the structure of type I procollagen in a patient who had osteogenesis imperfecta: excess mannose in the COOH-terminal propeptide.

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Authors

LPLeena PeltonenUniversity of HelsinkiAarno PalotieAarno PalotieStatens Serum InstitutDarwin J. ProckopDarwin J. ProckopRutgers, The State University of New Jersey

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Peltonen et al. (1980) studied this question.

synapsesocial.com/papers/6a730e7116009cf01ae0a98ahttps://doi.org/10.1073/pnas.77.10.6179
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Osteogenesis Imperfecta1977 · 26 citations
  2. 2Characterization of α1-Antitrypsin in the Inclusion Bodies from the Liver in α1-Antitrypsin Deficiency1975 · 116 citations
  3. 3Molecular abnormality of human alpha1-antitrypsin variant (Pi-ZZ) associated with plasma activity deficiency.1976 · 170 citations
  4. 4The Biosynthesis of Collagen and Its Disorders1979 · 579 citations