Deficiency of the syntrophins and α-dystrobrevin in patients with inherited myopathy

The syntrophins and dystrobrevins are members of the dystrophin-associated protein complex, and are thought to function as modular adaptors for signalling proteins recruited to the sarcolemmal membrane. We have characterised the expression of the syntrophins (α-, β1-, and β2-) and α-dystrobrevin by...

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Veröffentlicht in:	Neuromuscular disorders : NMD 2003-08, Vol.13 (6), p.456-467
Hauptverfasser:	Jones, K.J, Compton, A.G, Yang, N, Mills, M.A, Peters, M.F, Mowat, D, Kunkel, L.M, Froehner, S.C, North, K.N
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Alternative Splicing Blotting, Western Child, Preschool Cytoskeletal Proteins - analysis Cytoskeletal Proteins - deficiency Cytoskeletal Proteins - genetics DNA Mutational Analysis DNA, Complementary Dystrophin-Associated Proteins Female Humans Immunohistochemistry Infant Infant, Newborn Male Membrane Proteins - analysis Membrane Proteins - deficiency Membrane Proteins - genetics Muscle, Skeletal - chemistry Muscle, Skeletal - metabolism Muscle, Skeletal - pathology Muscular Dystrophies - genetics Muscular Dystrophies - metabolism Muscular Dystrophies - pathology Muscular dystrophy Myopathy Prospective Studies Retrospective Studies Syntrophins α-dystrobrevin
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