The second kindred with autosomal dominant distal myopathy linked to chromosome 14q: Genetic and clinical analysis

Archives of Neurology

Volumn 60, Issue 9, 2003, Pages 1321-1325

  Hedera, Peter ^a,d   Petty, Elizabeth M ^b   Bui, Melanie R ^a   Blaivas, Mila ^b   Fink, John K ^a,c  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^c VA ANN ARBOR HEALTHCARE SYSTEM   (United States)

^d VANDERBILT UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; MICROSATELLITE DNA; POLYADENYLATE BINDING PROTEIN 2; POLYADENYLIC ACID; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 14Q; CHROMOSOME 2P; CHROMOSOME 2Q; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE SEVERITY; DISTAL MYOPATHY; ELECTROMYOGRAM; EXTENSOR MUSCLE; FAMILIAL DISEASE; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENE SEGREGATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC RECOMBINATION; HAPLOTYPE; HEART DILATATION; HUMAN; HUMAN TISSUE; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; MUSCLE BIOPSY; MUSCLE WEAKNESS; MUTATIONAL ANALYSIS; ONSET AGE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TELOMERE;

ADULT; BIOPSY; CHROMOSOMES, HUMAN, PAIR 14; DNA MUTATIONAL ANALYSIS; ELECTROMYOGRAPHY; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; PEDIGREE; POINT MUTATION; POLY(A)-BINDING PROTEIN II; POLYMORPHISM, GENETIC;

EID: 0042421679     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.60.9.1321     Document Type: Article

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