(Q24311859)

GOA release 2020-03-11

muscle organ development

1 reference

GOA release 2020-03-11

author

Vincenzo Nigro

V Nigro

0 references

Mariz Vainzof

M Vainzof

4

0 references

Mayana Zatz

9

M Zatz

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Maria Rita Passos-Bueno

8

M R Passos-Bueno

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author name string

E de Sá Moreira

2

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G Piluso

3

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A Belsito

5

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L Politano

6

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A A Puca

https://scigraph.springernature.com/pub.10.1038/ng1096-195

7

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language of work or name

English

0 references

publication date

October 1996

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published in

Nature Genetics

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volume

14

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page(s)

195-8

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issue

2

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exact match

0 references

cites work

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/10.1038/NG1096-195

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1096-195

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

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/10.1038%2FNG1096-195

7 January 2021

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Dystrophin-associated proteins in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Human adhalin is alternatively spliced and the gene is located on chromosome 17q21

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Detection of a nonsense mutation in the dystrophin gene by multiple SSCP

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein

1 reference

https://api.crossref.org/works/10.1038%2FNG1096-195

7 January 2021