α-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy

Neuromuscular Disorders

Volumn 15, Issue 2, 2005, Pages 177-184

  Broccolini, Aldobrando ^a   Gliubizzi, Carla ^a   Pavoni, Ernesto ^a   Gidaro, Teresa ^a   Morosetti, Roberta ^a   Sciandra, Francesca ^a   Giardina, Bruno ^a   Tonali, Pietro ^a   Ricci, Enzo ^a,b   Brancaccio, Andrea ^a   Mirabella, Massimiliano ^a  

^a CATHOLIC UNIVERSITY   (Italy)

^b UILDM Rome Section   (Italy)

Author keywords

Dystroglycan; Dystrophin glycoprotein complex; GNE; HIBM; Inclusion body myopathy

Indexed keywords

DYSTROGLYCAN; DYSTROPHIN; GLYCOPROTEIN; LAMININ; LECTIN;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; FEMALE; GLYCOSYLATION; HUMAN; IMMUNOBLOTTING; IMMUNOCYTOCHEMISTRY; LECTIN BINDING; MALE; MOLECULAR WEIGHT; MUSCLE BIOPSY; MYOPATHY; MYOTUBE; PATHOGENESIS; PRIORITY JOURNAL; SIALYLATION; WHEAT GERM;

ADULT; CHROMOSOME DISORDERS; DOWN-REGULATION; DYSTROGLYCANS; FEMALE; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GLYCOSYLATION; HUMANS; IMMUNOHISTOCHEMISTRY; LAMININ; MALE; MIDDLE AGED; MUSCLE FIBERS; MUSCLE, SKELETAL; MYOSITIS, INCLUSION BODY; PROTEIN BINDING;

EID: 13444262055     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nmd.2004.10.001     Document Type: Article

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