Molecular Defects of the Disease-Causing Human Arrestin-1 C147F Mutant

PURPOSE: The purpose of this study was to identify the molecular defect in the disease-causing human arrestin-1 C147F mutant. METHODS: The binding of wild-type (WT) human arrestin-1 and several mutants with substitutions in position 147 (including C147F, which causes dominant retinitis pigmentosa in...

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Detalles Bibliográficos
Autores principales: Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2018
Materias:
Biochemistry and Molecular Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756042/
https://www.ncbi.nlm.nih.gov/pubmed/29305604
http://dx.doi.org/10.1167/iovs.17-22180

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756042/
https://www.ncbi.nlm.nih.gov/pubmed/29305604
http://dx.doi.org/10.1167/iovs.17-22180

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