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

1

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2 August 2017

Leturcq F

2

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Richard I

3

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Piccolo F

4

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Yalnizoglu D

5

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de Toma C

6

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Akçören Z

7

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Broux O

8

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Deburgrave N

9

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Brenguier L

10

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Roudaut C

11

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Urtizberea JA

12

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Jung D

13

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Tan E

14

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Jeanpierre M

15

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Campbell KP

16

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Kaplan JC

17

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Beckmann JS

18

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Topaloglu H

19

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publication date

1 August 1997

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2 August 2017

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2 August 2017

volume

42

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2 August 2017

issue

2

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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

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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

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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

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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

1 reference

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

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2 August 2017

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