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MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F
Known as:
LGMD1F
National Institutes of Health
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Related topics
Related topics
4 relations
Autosomal dominant inheritance
Cerebellar Nuclei
Rimmed vacuoles
Broader (1)
Muscular Dystrophies, Limb-Girdle
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Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Incomplete penetrance in limb‐girdle muscular dystrophy type 1F
M. Fanin
,
E. Peterle
,
+5 authors
C. Angelini
Muscle and Nerve
2015
Corpus ID: 206296195
Limb-girdle muscular dystrophy (LGMD) type 1F (MIM # 608423) is a rare autosomal dominant disorder whose locus was mapped and…
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2012
2012
Evaluation of Muscle Atrophy: Comparison between Limb-Girdle Muscular Dystrophies, ALS and Metabolic Myopathies (P07.197)
C. Angelini
,
M. Fanin
,
E. Peterle
2012
Corpus ID: 71319570
Objective: To study neuromuscular disorders by a quantitative measurement to evaluate muscle atrophy by MRI. Background The fibro…
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