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Sarcoglycan Complexes

Known as: Complex, Sarcoglycan, sarcoglycan-sarcospan complex location, sarcoglycan complex location 
A protein complex formed of four sarcoglycans plus sarcospan; there are six known sarcoglycans: alpha-, beta-, gamma-, delta-, epsilon- and zeta… Expand
National Institutes of Health

Papers overview

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Review
2004
Review
2004
The dystrophin glycoprotein complex (DGC) is a specialization of cardiac and skeletal muscle membrane. This large multicomponent… Expand
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Highly Cited
2000
Highly Cited
2000
Mutations in genes encoding for the sarcoglycans, a subset of proteins within the dystrophin–glycoprotein complex, produce a limb… Expand
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Highly Cited
2000
Highly Cited
2000
Two young males with limb-girdle muscular dystrophy (LGMD) resulting from sarcoglycan deficiency died at 27 (patient 1) and 18… Expand
Highly Cited
1999
Highly Cited
1999
To investigate mechanisms in the pathogenesis of cardiomyopathy associated with mutations of the dystrophin-glycoprotein complex… Expand
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Highly Cited
1999
Highly Cited
1999
beta-Sarcoglycan, one of the subunits of the sarcoglycan complex, is a transmembranous glycoprotein which associates with… Expand
Highly Cited
1998
Highly Cited
1998
Limb-girdle muscular dystrophy type 2D (LGMD 2D) is an autosomal recessive disorder caused by mutations in the α-sarcoglycan gene… Expand
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Highly Cited
1998
Highly Cited
1998
The sarcoglycans are a complex of four transmembrane proteins (α, β, γ, and δ) which are primarily expressed in skeletal muscle… Expand
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Review
1998
Review
1998
The involvement of the sarcoglycan complex in the pathogenesis of muscular dystrophy is becoming increasingly clear. Sarcoglycan… Expand
Highly Cited
1996
Highly Cited
1996
To enhance our understanding of the autosomal recessive limb-girdle muscular dystrophy (LGMD), patients from six genetically… Expand
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Highly Cited
1995
Highly Cited
1995
The dystrophin associated proteins (DAPs) are good candidates for harboring primary mutations in the genetically heterogeneous… Expand