On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers (Q58052179)

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English	On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers	article

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instance of

scholarly article

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title

On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers (English)

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main subject

heterozygosity

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based on heuristic

inferred from title

author

Vincenzo Nigro

object named as

Vincenzo Nigro

series ordinal

3

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author name string

Dirk Fischer

series ordinal

1

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Stefania Aurino

series ordinal

2

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Rolf Schröder

series ordinal

4

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publication date

15 October 2003

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published in

Annals of Neurology

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volume

54

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issue

5

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page(s)

674-678

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cites work

Making sense of the limb-girdle muscular dystrophies

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reference URL

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retrieved

21 January 2018

Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies

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reference URL

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21 January 2018

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

1 reference

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reference URL

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21 January 2018

The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies.

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.10738

retrieved

21 January 2018

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

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stated in

Crossref

reference URL

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retrieved

21 January 2018

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.10738

retrieved

21 January 2018

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.10738

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.10738

retrieved

21 January 2018

Mutations in the sarcoglycan genes in patients with myopathy

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Crossref

reference URL

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21 January 2018

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.

1 reference

stated in

Crossref

reference URL

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retrieved

21 January 2018

Consequences of a novel caveolin-3 mutation in a large German family

1 reference

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reference URL

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21 January 2018

Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island

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reference URL

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21 January 2018

Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities

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21 January 2018

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

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reference URL

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retrieved

21 January 2018

Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria

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stated in

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reference URL

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retrieved

21 January 2018

Facioscapulohumeral dystrophy

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stated in

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reference URL

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retrieved

21 January 2018

Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study

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Crossref

reference URL

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retrieved

21 January 2018

Identifiers

DOI

10.1002/ANA.10738

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PubMed publication ID

14595658

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