Open AccessMolecular Defects of the Disease-Causing Human Arrestin-1 C147F Mutant
Author(s) -
Sergey A. Vishnivetskiy,
Lori S. Sullivan,
Sara J. Bowne,
Stephen P. Daiger,
Eugenia V. Gurevich,
Vsevolod V. Gurevich
Publication year - 2018
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.17-22180
Subject(s) - arrestin , rhodopsin , mutant , retinitis pigmentosa , mutant protein , wild type , retinal degeneration , mutation , microbiology and biotechnology , biology , protein aggregation , chemistry , hek 293 cells , biochemistry , signal transduction , retinal , gene , g protein coupled receptor
The purpose of this study was to identify the molecular defect in the disease-causing human arrestin-1 C147F mutant.
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