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A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.
Academic Article
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Cardiomyopathy of limb-girdle muscular dystrophy.
Academic Article
Why?
Muscular Dystrophies, Limb-Girdle
Concept
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Dysferlin deficiency and the development of cardiomyopathy in a mouse model of limb-girdle muscular dystrophy 2B.
Academic Article
Why?
Wolfe, Scot
Person
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Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation.
Academic Article
Why?
Magnetic Resonance Imaging Is Sensitive to Pathological Amelioration in a Model for Laminin-Deficient Congenital Muscular Dystrophy (MDC1A).
Academic Article
Why?
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
Academic Article
Why?
Precise therapeutic gene correction by a simple nuclease-induced double-stranded break.
Academic Article
Why?
Brown, Robert
Person
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Dominov, Janice
Person
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Iyer, Sukanya
Person
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Shultz, Leonard
Person
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Emerson, Charles
Person
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King, Oliver
Person
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