Cargando…
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta
Heat shock protein 47 (HSP47), encoded by the SERPINH1 gene, is a molecular chaperone essential for correct folding of collagens. We report a homozygous p.(R222S) substitution in HSP47 in a child with severe osteogenesis imperfecta leading to early demise. p.R222 is a highly conserved residue locate...
Autores principales: | Syx, Delfien, Ishikawa, Yoshihiro, Gebauer, Jan, Boudko, Sergei P., Guillemyn, Brecht, Van Damme, Tim, D’hondt, Sanne, Symoens, Sofie, Nampoothiri, Sheela, Gould, Douglas B., Baumann, Ulrich, Bächinger, Hans Peter, Malfait, Fransiska |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7877763/ https://www.ncbi.nlm.nih.gov/pubmed/33524049 http://dx.doi.org/10.1371/journal.pgen.1009339 |
Ejemplares similares
-
Loss of TANGO1 Leads to Absence of Bone Mineralization
por: Guillemyn, Brecht, et al.
Publicado: (2021) -
The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review
por: Colman, Marlies, et al.
Publicado: (2019) -
Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans
por: Symoens, Sofie, et al.
Publicado: (2013) -
Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndrome
por: Malfait, Fransiska, et al.
Publicado: (2013) -
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta
por: van Dijk, Fleur S, et al.
Publicado: (2012)