Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies: 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands

Neuromuscular Disorders

Volumn 13, Issue 7-8, 2003, Pages 589-596

  Udd, B ^a   Meola, G ^a   Krahe, R ^a   Thornton, C ^a   Ranum, L ^a   Day, J ^a   Bassez, G ^a   Ricker, K ^a  

^a VAASA CENTRAL HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; CONFERENCE PAPER; CREATINE KINASE BLOOD LEVEL; DIAGNOSTIC PROCEDURE; DISEASE COURSE; EVALUATION; GENE EXPRESSION; GENE LOCUS; GENE MAPPING; GENE MUTATION; HUMAN; IN SITU HYBRIDIZATION; MUSCLE BIOPSY; MUTATIONAL ANALYSIS; MYOTONIC DYSTROPHY; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROXIMAL MYOTONIC MYOPATHY; SOUTHERN BLOTTING; SYMPTOMATOLOGY;

EID: 0043073111     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(03)00092-0     Document Type: Conference Paper

References (10)

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8. Meola G., Udd B., Sansone V., Ptacek L., Lee D., Krahe R. Dominant multi-system proximal myotonic myopathic syndromes: clinical and genetic heterogeneity in three families (Abstract). Neurology. 52:(Suppl. 2):1999;A95.
9. Liquori C.L., Ricker K., Moseley M.L., et al. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science. 293:(5531):2001;864-867.
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