Secondary calpain3 deficiency in 2q-linked muscular dystrophy: Titin is the candidate gene

Neurology

Volumn 56, Issue 7, 2001, Pages 869-877

  Haravuori, H ^a   Vihola, A ^c   Straub, V ^h   Auranen, M ^a   Richard, I ^f   Marchand, S ^f   Voit, T ^d   Labeit, S ^e   Somer, H ^b   Peltonen, L ^a,g   Beckmann, J S ^f   Udd, B ^c  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

^c VAASA CENTRAL HOSPITAL   (Finland)

^d UNIVERSITY OF DUISBURG ESSEN   (Germany)

^e Faculty of Clinical Medicine   (Germany)

^f GÉNÉTHON   (France)

^g UNIVERSITY OF CALIFORNIA   (United States)

^h NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALPAIN; CALPAIN 3; CONNECTIN; I KAPPA B; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; UNCLASSIFIED DRUG;

ANIMAL TISSUE; APOPTOSIS; ARTICLE; CHROMOSOME 2Q; CHROMOSOME MUTATION; CONTROLLED STUDY; ENZYME DEFICIENCY; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC LINKAGE; HAPLOTYPE; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LIMB GIRDLE MUSCULAR DYSTROPHY; MOUSE; MUSCULAR DYSTROPHY; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SOUTHERN BLOTTING; TIBIA; TIBIA MUSCULAR DYSTROPHY; WESTERN BLOTTING;

EID: 0035836751     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.7.869     Document Type: Article

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