Impacts of two point mutations of RPE65 from Leber's congenital amaurosis on the stability, subcellular localization and isomerohydrolase activity of RPE65

FEBS Letters

Volumn 580, Issue 17, 2006, Pages 4200-4204

  Chen, Ying ^a   Moiseyev, Gennadiy ^a   Takahashi, Yusuke ^a   Ma, Jian xing ^a  

^a UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

Author keywords

LRAT; Retinal degeneration; Retinoid; RPE; RPE65; Visual cycle

Indexed keywords

HYDROLASE; MEMBRANE PROTEIN; PROTEIN RPE65; UNCLASSIFIED DRUG;

ARTICLE; CONGENITAL BLINDNESS; ENZYME ACTIVITY; HUMAN; HUMAN CELL; POINT MUTATION; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN STABILITY; VISUAL IMPAIRMENT;

AMINO ACID SUBSTITUTION; BLINDNESS; CARRIER PROTEINS; CELL LINE; CIS-TRANS-ISOMERASES; EYE PROTEINS; HUMANS; OPTIC ATROPHY, HEREDITARY, LEBER; PIGMENT EPITHELIUM OF EYE; POINT MUTATION; PROTEIN TRANSPORT; RETINALDEHYDE;

EID: 33745865867     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2006.06.078     Document Type: Article

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