The fibril core of transforming growth factor beta-induced protein (TGFBIp) facilitates aggregation of corneal TGFBIp

Mutations in the transforming growth factor beta-induced (TGFBI) gene result in a group of hereditary diseases of the cornea that are collectively known as TGFBI corneal dystrophies. These mutations translate into amino acid substitutions mainly within the fourth fasciclin 1 domain (FAS1-4) of the t...

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Vydáno v:Biochemistry
Hlavní autoři: Sørensen, Charlotte S., Runager, Kasper, Scavenius, Carsten, Jensen, Morten M., Nielsen, Nadia S., Christiansen, Gunna, Petersen, Steen V., Karring, Henrik, Sanggaard, Kristian W., Enghild, Jan J.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4789106/
https://ncbi.nlm.nih.gov/pubmed/25910219
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.biochem.5b00292
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