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MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F

Known as: LGMD1F 
National Institutes of Health

Papers overview

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2015
2015
Limb-girdle muscular dystrophy (LGMD) type 1F (MIM # 608423) is a rare autosomal dominant disorder whose locus was mapped and… Expand
Review
2014
Review
2014
Limb-girdle muscular dystrophies (LGMD) are a highly heterogeneous group of muscle disorders, which first affect the voluntary… Expand
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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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2013
2013
Of the seven autosomal dominant genetically distinct forms of LGMD so far described, in only four the causative gene has been… Expand
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2012
2012
Objective: To study neuromuscular disorders by a quantitative measurement to evaluate muscle atrophy by MRI. Background The fibro… Expand
2004
2004
ZusammenfassungGliedergürteldystrophien (limb girdle muscular dystrophies, LGMD) sind genetisch heterogene, primäre Myopathien… Expand