Minimal expansion of the gcg repeat in the pabp2 gene does not predispose to sporadic inclusion body myositis

Neurology

Volumn 52, Issue 3, 1999, Pages 669-670

  Mezei, M M ^a   Mankodi, A ^a   Brais, B ^a   Marineau, C ^a   Thornton, C A ^a   Rouleau, G A ^a   Karpati, G ^a  

^a NONE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; POLYADENYLIC ACID;

ARTICLE; CHROMOSOME 14; CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; GENE MUTATION; GENETIC PREDISPOSITION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INCLUSION BODY MYOSITIS; MUSCLE BIOPSY; OCULOPHARYNGEAL MUSCULAR DYSTROPHY; PRIORITY JOURNAL; RECESSIVE GENE; TRINUCLEOTIDE REPEAT;

EID: 0033016948     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.3.669     Document Type: Article

References (7)