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Corneal Dystrophy-associated R124H Mutation Disrupts TGFBI Interaction with Periostin and Causes Mislocalization to the Lysosome

The 5q31-linked corneal dystrophies are heterogeneous autosomal-dominant eye disorders pathologically characterized by the progressive accumulation of aggregated proteinaceous deposits in the cornea, which manifests clinically as severe vision impairment. The 5q31-linked corneal dystrophies are comm...

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Bibliografski detalji
Glavni autori: Kim, Bong-Yoon, Olzmann, James A., Choi, Seung-il, Ahn, So Yeon, Kim, Tae-im, Cho, Hyun-Soo, Suh, Hwal, Kim, Eung Kweon
Format: Artigo
Jezik:Inglês
Izdano: American Society for Biochemistry and Molecular Biology 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2740584/
https://ncbi.nlm.nih.gov/pubmed/19478074
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M109.013607
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