Abnormal lysosomal and ubiquitin-proteasome pathways in 19p13.3 distal myopathy

Annals of Neurology

Volumn 56, Issue 1, 2004, Pages 133-138

  Di Blasi, Claudia ^a   Moghadaszadeh, Behzad ^b   Ciano, Claudia ^a   Negri, Tiziana ^a   Giavazzi, Alessio ^a   Cornelio, Ferdinando ^a   Morandi, Lucia ^a   Mora, Marina ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

^b BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEASOME; UBIQUITIN;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL VACUOLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 19P; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; DISTAL MYOPATHY; ETHNOLOGY; GENE LOCUS; GENETIC MARKER; GENOTYPE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOCHEMISTRY; LINKAGE ANALYSIS; LYSOSOME; MUSCLE WEAKNESS; NUCLEOTIDE SEQUENCE; ONSET AGE; PRIORITY JOURNAL; PROTEIN DEGRADATION;

ADULT; BIOLOGICAL MARKERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; CYSTEINE ENDOPEPTIDASES; HUMANS; LINKAGE (GENETICS); LYSOSOMES; MIDDLE AGED; MULTIENZYME COMPLEXES; MUSCLE PROTEINS; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; PEDIGREE; PROTEASOME ENDOPEPTIDASE COMPLEX; UBIQUITIN; VACUOLES;

EID: 3042796433     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20158     Document Type: Article

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