Limb-girdle Muscular Dystrophies in India: A Review. - Wikidata - awgldk - TriplyDB

Limb-girdle Muscular Dystrophies in India: A Review.

Limb-girdle Muscular Dystrophies in India: A Review.

http://www.wikidata.org/entity/Q33795491

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The clinical spectrum and genetic variability of limb-girdle muscular dystrophy in a cohort of Chinese patients

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Limb-girdle Muscular Dystrophies in India: A Review.

http://www.wikidata.org/entity/Q33795491

description

2017 nî lūn-bûn

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2017 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2017 թվականի ապրիլին հրատարակված գիտական հոդված

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

@zh-hk

2017年論文

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2017年論文

@zh-tw

2017年论文

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name

Limb-girdle Muscular Dystrophies in India: A Review.

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Limb-girdle Muscular Dystrophies in India: A Review.

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type

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Limb-girdle Muscular Dystrophies in India: A Review.

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Limb-girdle Muscular Dystrophies in India: A Review.

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Limb-girdle Muscular Dystrophies in India: A Review.

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Limb-girdle Muscular Dystrophies in India: A Review.

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AIAN.AIAN_81_17

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Annals of Indian Academy of Neurology

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Limb-girdle Muscular Dystrophies in India: A Review.

@en

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Hinaben Dayalal Faldu

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Rakesh Singh

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Sarika Bapuso Patil

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Satish V Khadilkar

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P2860

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

Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)

Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)

Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy

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87-95

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scholarly article

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10.4103/AIAN.AIAN_81_17

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2

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20

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5470147

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