Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy

Current Neurology and Neuroscience Reports

Volumn 5, Issue 1, 2005, Pages 61-65

  Nonaka, Ikuya ^a   Noguchi, Satoru ^a   Nishino, Ichizo ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CELL MEMBRANE PROTEIN; CREATININE; EPIMERASE; SIALIC ACID; URIDINE DIPHOSPHATE N ACETYLGLUCOSAMINE;

ACYLATION; ALLELE; ALLOSTERISM; AUTOSOMAL RECESSIVE INHERITANCE; BINDING SITE; CELL INCLUSION; CELL VACUOLE; CHROMOSOME 9; CHROMOSOME MAP; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CREATININE BLOOD LEVEL; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE PREDISPOSITION; DISTAL MYOPATHY; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ETHNIC DIFFERENCE; ETHNIC GROUP; GAIT DISORDER; GENE FUNCTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC CORRELATION; GENETIC LINKAGE; GENETIC MODEL; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; GLYCOSYLATION; HISTOPATHOLOGY; HUMAN; INCLUSION BODY MYOSITIS; MARINESCO SJOGREN SYNDROME; MISSENSE MUTATION; MUSCLE ATROPHY; MUSCLE BIOPSY; MUSCLE DISEASE; MUSCLE NECROSIS; MUSCLE WEAKNESS; MUTATIONAL ANALYSIS; NICK END LABELING; OCULOPHARYNGEAL MUSCULAR DYSTROPHY; ONSET AGE; PATHOGENESIS; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FUNCTION; QUADRICEPS FEMORIS MUSCLE; REVIEW; SIALYLATION; SIGNAL TRANSDUCTION;

EID: 16344367073     PISSN: 15284042     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11910-005-0025-0     Document Type: Review

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