MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B

Known as: Muscular dystrophy, limb-girdle, type 3, LGMD3, LGMD2B 
 
National Institutes of Health

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Highly Cited
2010
Highly Cited
2010
The recently described human anion channel Anoctamin (ANO) protein family comprises at least ten members, many of which have been… (More)
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Highly Cited
2008
Highly Cited
2008
Dysferlin deficiency causes limb-girdle muscular dystrophy type 2B (LGMD2B; proximal weakness) and Miyoshi myopathy (distal… (More)
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Highly Cited
2008
Highly Cited
2008
Limb girdle muscular dystrophies (LGMD) are characterized by genetic and clinical heterogeneity: seven autosomal dominant and 12… (More)
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2004
2004
A 57-year-old woman first noticed difficulty in walking at the age of 34 years, and since then muscle wasting and weakness in the… (More)
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2001
2001
Dysferlin is the protein product of the DYSF gene mapped at 2p31, which mutations cause limb-girdle muscular dystrophy type 2B… (More)
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Highly Cited
2000
Highly Cited
2000
Limb-girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi myopathy (MM) are autosomal recessive disorders caused by mutations… (More)
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Highly Cited
2000
Highly Cited
2000
Dysferlin has recently been identified as a novel gene involved in limb-girdle muscular dystrophy type 2B (LGMD2B) and its… (More)
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Highly Cited
1999
Highly Cited
1999
Limb girdle muscular dystrophy type 2B (LGMD2B) and Miyoshi myopathy (MM), a distal muscular dystrophy, are both caused by… (More)
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1999
1999
The autosomal recessive limb-girdle muscular dystrophies (AR-LGMDs) are a heterogeneous group of disorders of progressive… (More)
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Highly Cited
1996
Highly Cited
1996
Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of inherited neuromuscular disorders characterized by proximal… (More)
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