Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2

Muscle and Nerve

Volumn 35, Issue 2, 2007, Pages 259-264

  Toth, Cory ^a   Dunham, Chris ^a   Suchowersky, Oksana ^a   Parboosingh, Jillian ^a   Brownell, Keith ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

Hereditary myopathy; Muscle pathology; Myotonia; Myotonic dystrophy type II; Vacuoles

Indexed keywords

DNA; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN; ZINC FINGER PROTEIN 9;

ADULT; ARTICLE; CASE REPORT; DIAGNOSTIC VALUE; FAMILIAL DISEASE; FEMALE; GENE; HISTOPATHOLOGY; HUMAN; INTRON; MALE; MOLECULAR GENETICS; MUSCLE BIOPSY; MYOTONIC DYSTROPHY; MYOTONIC DYSTROPHY TYPE 2; NUCLEOTIDE REPEAT; PHENOTYPE; POLAND; PRIORITY JOURNAL; RELATIVE; SARCOLEMMA; ZNF9 GENE;

ADULT; DNA MUTATIONAL ANALYSIS; DNA REPEAT EXPANSION; FEMALE; HUMANS; MALE; MICROSCOPY, ELECTRON, TRANSMISSION; MIDDLE AGED; MUSCLE, SKELETAL; MYOTONIC DYSTROPHY; PEDIGREE; RNA-BINDING PROTEINS; SARCOLEMMA;

EID: 33847006605     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.20685     Document Type: Article

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