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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...
Autores principales: | Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2018
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Materias: | |
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 |
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