Juvenile neuronal ceroid-lipofuscinosis (Batten disease): A brief review and update

Current Molecular Medicine

Volumn 7, Issue 6, 2007, Pages 603-608

  Rakheja, Dinesh ^a   Narayan, Srinivas B ^b   Bennett, Michael J ^c  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Bis(monoacylglycerol)phosphate; Congenital neuronal ceroid lipofuscinosis; Neuronal cytoplasm; Santavuori Haltia disease; Synaptosomes

Indexed keywords

LYSOBISPHOSPHATIDIC ACID; MEMBRANE PROTEIN; MONOACYLGLYCEROL; PALMITOYL PROTEIN DELTA 9 DESATURASE; PROTEIN CLN3; UNCLASSIFIED DRUG;

APOPTOSIS; BRAIN ATROPHY; CEREBELLUM ATROPHY; CHROMOSOME 16P; CLINICAL FEATURE; COGNITIVE DEFECT; DYSARTHRIA; GENE DELETION; GENE DUPLICATION; GENE MUTATION; HETEROZYGOSITY; HISTOPATHOLOGY; HUMAN; LIPID RAFT; MENTAL DISEASE; MOLECULAR GENETICS; MOTOR DYSFUNCTION; NEURONAL CEROID LIPOFUSCINOSIS; NEUROPATHOLOGY; NONHUMAN; PALMITOYLATION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; RETINA MACULA DEGENERATION; REVIEW; SEIZURE; SLEEP DISORDER; VISUAL ACUITY;

ANIMALS; FATTY ACID DESATURASES; HUMANS; NEURONAL CEROID-LIPOFUSCINOSES;

EID: 35448976080     PISSN: 15665240     EISSN: None     Source Type: Journal    
DOI: 10.2174/156652407781695729     Document Type: Review

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