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Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta

Osteogenesis imperfecta (OI) is a heritable connective tissue disease characterized by bone fragility and increased risk of fractures. Up to now, mutations in at least 18 genes have been associated with dominant and recessive forms of OI that affect the production or post-translational processing of...

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Dades bibliogràfiques
Publicat a:J Biol Chem
Autors principals: Lindert, Uschi, Weis, Mary Ann, Rai, Jyoti, Seeliger, Frank, Hausser, Ingrid, Leeb, Tosso, Eyre, David, Rohrbach, Marianne, Giunta, Cecilia
Format: Artigo
Idioma:Inglês
Publicat: American Society for Biochemistry and Molecular Biology 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4505018/
https://ncbi.nlm.nih.gov/pubmed/26004778
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M115.661025
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