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A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.Academic Article Why?
Cardiomyopathy of limb-girdle muscular dystrophy.Academic Article Why?
Muscular Dystrophies, Limb-GirdleConcept Why?
Dysferlin deficiency and the development of cardiomyopathy in a mouse model of limb-girdle muscular dystrophy 2B.Academic Article Why?
Wolfe, ScotPerson Why?
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, RobertPerson Why?
Dominov, JanicePerson Why?
Girgenrath, MahaswetaPerson Why?
Shultz, LeonardPerson Why?
Emerson, CharlesPerson Why?
King, OliverPerson Why?
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