HSP47 and FKBP65 cooperate in the synthesis of type I procollagen

Osteogenesis imperfecta (OI) is a genetic disorder that results in low bone mineral density and brittle bones. Most cases result from dominant mutations in the type I procollagen genes, but mutations in a growing number of genes have been identified that produce autosomal recessive forms of the dise...

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Bibliografiske detaljer
Udgivet i:Hum Mol Genet
Main Authors: Duran, Ivan, Nevarez, Lisette, Sarukhanov, Anna, Wu, Sulin, Lee, Katrina, Krejci, Pavel, Weis, Maryann, Eyre, David, Krakow, Deborah, Cohn, Daniel H.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2015
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4355024/
https://ncbi.nlm.nih.gov/pubmed/25510505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu608
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