Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation (Q24675581)

2

object named as

M R Passos-Bueno

0 references

author name string

E M McNally

1

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C G Bönnemann

3

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M Vainzof

4

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E de Sá Moreira

5

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H G Lidov

6

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K B Othmane

7

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P H Denton

8

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J M Vance

9

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L M Kunkel

American Journal of Human Genetics

11

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language of work or name

English

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publication date

November 1996

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published in

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volume

59

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issue

5

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page(s)

1040-7

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cites work

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

1 reference

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Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)

7 April 2017

1 reference

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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914841

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency

7 April 2017

1 reference

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

7 April 2017

1 reference

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A simple salting out procedure for extracting DNA from human nucleated cells

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914841

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

7 April 2017

1 reference

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Cloning of human microtubule-associated protein 1B and the identification of a related gene on chromosome 15

7 April 2017

1 reference

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

7 April 2017

1 reference

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

7 April 2017

1 reference

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

7 April 2017

1 reference

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Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

28 September 2017

1 reference

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Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

28 September 2017

1 reference

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

28 September 2017

1 reference

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Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914841

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

28 November 2018

1 reference

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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

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8900232

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

3500915

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference

3500915

PubMed publication ID

8900232

1 reference

Consolidated OpenCitations Corpus – April 2017