Decreased plasma carnitine and trimethyl-L-lysine levels associated with lysosomal accumulation of a trimethyl-L-lysine containing protein in Batten disease

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1317, Issue 3, 1996, Pages 192-198

  Katz, Martin L ^a  

^a University of Missouri   (United States)

Author keywords

Batten disease; Carnitine; Ceroid lipofuscinosis; Hereditary disease; Lysosomal storage disease; Metabolic defect; Protein modification; Trimethyllysine

Indexed keywords

CARNITINE; MEMBRANE PROTEIN; PROTEIN SUBUNIT; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

AMINO ACID SEQUENCE; ARTICLE; BLOOD ANALYSIS; CONTROLLED STUDY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HISTOCHEMISTRY; HUMAN; HUMAN TISSUE; LYSOSOME STORAGE DISEASE; NEURONAL CEROID LIPOFUSCINOSIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEGRADATION; PROTEIN METHYLATION; SIGNAL TRANSDUCTION;

ADULT; CARNITINE; CHILD; FEMALE; HETEROZYGOTE; HUMANS; LYSINE; MALE; NEURONAL CEROID-LIPOFUSCINOSES;

EID: 0030590877     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(96)00054-3     Document Type: Article

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