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Muscular dystrophy, limb-girdle, type 1A

Known as: Muscular Dystrophy, Limb-Girdle, Type1A, LGMD1A, MUSCULAR DYSTROPHY, PROXIMAL, TYPE 1A 
 
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetically determined muscle disorders with a primary or… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND AND OBJECTIVE The term myofibrillar myopathy (MFM) is a noncommittal term for a pathologic pattern of myofibrillar… Expand
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Highly Cited
2000
Highly Cited
2000
We have identified a mutation in the myotilin gene in a large North American family of German descent expressing an autosomal… Expand
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2000
2000
The lobula giant movement detector (LGMD1 and -2) neurons in the locust visual system are parts of motion-sensitive pathways that… Expand
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Highly Cited
1999
Highly Cited
1999
The striated muscle sarcomeres are highly organized structures composed of actin (thin) and myosin (thick) filaments that slide… Expand
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1999
1999
We report the identification of a new locus for autosomal dominant limb-girdle muscular dystrophy (LGMD1) on 7q. Two of five… Expand
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Highly Cited
1998
Highly Cited
1998
Limb-girdle muscular dystrophy (LGMD) is a clinically and genetically heterogeneous group of myopathies, including autosomal… Expand
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Highly Cited
1997
Highly Cited
1997
Limb-girdle muscular dystrophy (LGMD) constitutes a clinically and genetically heterogeneous group of myogenic disorders with a… Expand
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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… Expand
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1996
1996
Limb-girdle muscular dystrophies (LGMDs) represent a clinically heterogeneous group of genetic diseases characterised by… Expand
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