A model for Batten disease protein CLN3: Functional implications from homology and mutations

FEBS Letters

Volumn 399, Issue 1-2, 1996, Pages 75-77

  Janes, Robert W ^a,c   Munroe, Patricia B ^b   Mitchison, Hannah M ^b   Gardiner, R Mark ^b   Mole, Sara E ^b   Wallace, B A ^a  

^a UNIVERSITY OF LONDON   (United Kingdom)

^b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^c QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

Chaperone; Genetic disease; Membrane protein; Molecular modeling; Neurodegenerative disease

Indexed keywords

CHAPERONE; MEMBRANE PROTEIN; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

AMINO ACID SEQUENCE; ARTICLE; GENETIC CONSERVATION; HUMAN; MITOCHONDRIAL MEMBRANE; MODEL; MOLECULAR MODEL; MUTATION; NEURONAL CEROID LIPOFUSCINOSIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FOLDING; SEQUENCE HOMOLOGY; YEAST;

AMINO ACID SEQUENCE; CYCLINS; HUMANS; MEMBRANE GLYCOPROTEINS; MOLECULAR CHAPERONES; MOLECULAR SEQUENCE DATA; MUTATION; NEURONAL CEROID-LIPOFUSCINOSES; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0030577376     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(96)01290-2     Document Type: Article

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