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Article

Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease.

Journal of neurology, neurosurgery, and psychiatry - 1 Jun 2008

Traverso M, Bruno C, Broccolini A, Sotgia F, Donati M A, Assereto S, Gazzerro E, Lo Monaco M, Modoni A, D'Amico A, Gasperini S, Ricci E, Zara F, Lisanti M, Minetti C

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Caveolin 3
Creatine Kinase
Electromyography
Muscle Contraction
Muscle Weakness
Muscular Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Neurologic Examination

Receptors, Oxytocin

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PMID: 18487559
DOI: 10.1136/jnnp.2007.133207

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Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease.PMID 18487559Read ↗

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Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases.Semantic proximity Read ↗

A new missense mutation in caveolin-3 gene causes rippling muscle disease.Semantic proximity Read ↗

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Caveolinopathies: translational implications of caveolin-3 in skeletal and cardiac muscle disorders.Semantic proximity Read ↗

Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene.Semantic proximity Read ↗

Consequences of a novel caveolin-3 mutation in a large German family.Semantic proximity Read ↗

The spectrum of rippling muscle diseaseSemantic proximity Read ↗

A Role for Caveolin-3 in the Pathogenesis of Muscular Dystrophies.Semantic proximity Read ↗

Phenotypic behavior of caveolin-3 R26Q, a mutant associated with hyperCKemia, distal myopathy, and rippling muscle disease.Semantic proximity Read ↗

Caveolin-3 gene mutation in Japanese with rippling muscle disease.Semantic proximity Read ↗

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