Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review). - sprookjes - yvandenbroek - TriplyDB

Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).

Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).

http://www.wikidata.org/entity/Q33608787

about

Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt.Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation.Concise review: mesoangioblast and mesenchymal stem cell therapy for muscular dystrophy: progress, challenges, and future directions.Quality of life in adult patients with limb-girdle muscular dystrophies.LGMD2E is the most common type of sarcoglycanopathies in the Iranian population.Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet.Bethlem myopathy in a Portuguese patient - case report.

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P2860

Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).

http://www.wikidata.org/entity/Q33608787

description

2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Limb-girdle muscular dystrophi ...... m the first proposal (Review).

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Limb-girdle muscular dystrophi ...... m the first proposal (Review).

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Limb-girdle muscular dystrophi ...... m the first proposal (Review).

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Limb-girdle muscular dystrophi ...... m the first proposal (Review).

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Limb-girdle muscular dystrophi ...... m the first proposal (Review).

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Molecular Medicine Reports

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Limb-girdle muscular dystrophi ...... m the first proposal (Review).

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Omar A Mahmood

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Xin Mei Jiang

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Creative Commons Attribution 3.0 Unported

P2860

Myotilin is mutated in limb girdle muscular dystrophy 1A

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy

Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Immunohistochemical analysis of calpain 3: advantages and limitations in diagnosing LGMD2A

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.

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10.3892/MMR.2014.2048

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limb-girdle muscular dystrophy

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