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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1994-2018
051019942018

Papers overview

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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… (More)
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Highly Cited
2000
Highly Cited
2000
The sarcoglycan complex is composed of four membrane-spanning dystrophin-associated proteins (DAPs) and is essential for skeletal… (More)
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2000
2000
Two young males with limb-girdle muscular dystrophy (LGMD) resulting from sarcoglycan deficiency died at 27 (patient 1) and 18… (More)
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Highly Cited
2000
Highly Cited
2000
Limb-girdle muscular dystrophy type 2E (LGMD 2E) is caused by mutations in the beta-sarcoglycan gene, which is expressed in… (More)
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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… (More)
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Highly Cited
1998
Highly Cited
1998
Limb-girdle muscular dystrophy type 2D (LGMD 2D) is an autosomal recessive disorder caused by mutations in the alpha-sarcoglycan… (More)
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1998
1998
Four types of limb-girdle muscular dystrophy (LGMD) are known to be caused by mutations in distinct sarcoglycan genes. The BIO 14… (More)
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1998
1998
The sarcoglycans are a complex of four transmembrane proteins (alpha, beta, gamma, and delta) which are primarily expressed in… (More)
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Highly Cited
1996
Highly Cited
1996
To enhance our understanding of the autosomal recessive limb-girdle muscular dystrophy (LGMD), patients from six genetically… (More)
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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… (More)
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