(Q34436405)

2 August 2017

title

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey (English)

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2 August 2017

Dinçer P

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2 August 2017

Leturcq F

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2 August 2017

Richard I

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2 August 2017

Piccolo F

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2 August 2017

Yalnizoglu D

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2 August 2017

de Toma C

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2 August 2017

Akçören Z

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2 August 2017

Broux O

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2 August 2017

Deburgrave N

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2 August 2017

Brenguier L

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2 August 2017

Roudaut C

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2 August 2017

Urtizberea JA

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2 August 2017

Jung D

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2 August 2017

Tan E

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2 August 2017

Jeanpierre M

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2 August 2017

Campbell KP

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2 August 2017

Kaplan JC

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2 August 2017

Beckmann JS

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2 August 2017

Topaloglu H

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2 August 2017

publication date

1 August 1997

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2 August 2017

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2 August 2017

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2 August 2017

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2 August 2017

page(s)

222-229

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Population frequencies of inherited neuromuscular diseases—A world survey

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

The limb-girdle muscular dystrophies--proposal for a new nomenclature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

The 1993-94 Généthon human genetic linkage map

21 January 2018

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https://api.crossref.org/works/10.1002%2FANA.410420214

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

From adhalinopathies to alpha-sarcoglycanopathies: an overview.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410420214

21 January 2018

Identifiers

DOI

10.1002/ANA.410420214

1 reference

2 August 2017

1 reference