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A lethal variant of osteogenesis imperfecta has a single base mutation that substitutes cysteine for glycine 904 of the alpha 1(I) chain of type I procollagen. The asymptomatic mother has an unidentified mutation producing an overmodified and unstable type I procollagen.

A fraction of the pro alpha 1(I) and pro alpha 2(I) chains in type I procollagen synthesized by the fibroblasts from a proband with a lethal variant of osteogenesis imperfecta were overmodified by posttranslational reactions. After digestion with pepsin, some of the alpha 1(I) chains were recovered...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Principais autores: Constantinou, C D, Nielsen, K B, Prockop, D J
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1989
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC303717/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2913053/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113920
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