(Q38978151)

8 September 2017

title

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3. (English)

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autosomal recessive limb-girdle muscular dystrophy

8 September 2017

main subject

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author name string

Driss A

1

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8 September 2017

Amouri R

2

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8 September 2017

Ben Hamida C

3

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8 September 2017

Souilem S

4

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8 September 2017

Gouider-Khouja N

5

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8 September 2017

Ben Hamida M

6

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8 September 2017

Hentati F

7

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8 September 2017

publication date

1 June 2000

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8 September 2017

published in

Neuromuscular Disorders

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8 September 2017

volume

10

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8 September 2017

issue

4-5

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8 September 2017

page(s)

240-246

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

8 September 2017

cites work

1 reference

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7 January 2021

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

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7 January 2021

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

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

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7 January 2021

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

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

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

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

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

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7 January 2021

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12

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7 January 2021

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

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

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7 January 2021

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

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7 January 2021

Muscular dystrophies and the dystrophin-glycoprotein complex

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

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

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7 January 2021

Abnormal expression of heparin sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency

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7 January 2021

Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1.

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7 January 2021

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

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7 January 2021

Strategies for multilocus linkage analysis in humans

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

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7 January 2021

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

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7 January 2021

(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein

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7 January 2021

beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations

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7 January 2021

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

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7 January 2021

Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex

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https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

A foundation for limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

Mapping of human interferon regulatory factor 3 (IRF3) to chromosome 19q13.3-13.4 by an intragenic polymorphic marker

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900099-7

7 January 2021

10.1016/S0960-8966(00)00099-7

Identifiers

DOI

1 reference

8 September 2017

1 reference