Immunoblot as a potential diagnostic tool for myofibrillar myopathies.

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Immunoblot as a potential diagnostic tool for myofibrillar myopathies.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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Immunoblot as a potential diagnostic tool for myofibrillar myopathies.

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Immunoblot as a potential diagnostic tool for myofibrillar myopathies.

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Immunoblot as a potential diagnostic tool for myofibrillar myopathies.

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P1476

Immunoblot as a potential diagnostic tool for myofibrillar myopathies

@en

P2093

Georgine Faulkner

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Giuliano Tomelleri

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Matteo Marini

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Silvio Piffer

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P2860

Sample prep for proteomics of breast cancer: proteomics and gene ontology reveal dramatic differences in protein solubilization preferences of radioimmunoprecipitation assay and urea lysis buffers

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

Mutations in myotilin cause myofibrillar myopathy

Myofibrillar myopathies

Mutations in ZASP define a novel form of muscular dystrophy in humans

The prion protein in human neuromuscular diseases.

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

Mutation in BAG3 causes severe dominant childhood muscular dystrophy.

Myofibrillar myopathies: a clinical and myopathological guide.

P304

3097-3100

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P31

scholarly article

P356

10.1002/ELPS.201500277

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Gaetano Vattemi

Valeria Guglielmi

P577

2015-10-20T00:00:00Z

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P698

26383991

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