Exon deletion pattern in duchene muscular dystrophy in north west of iran (Q35576460)

8 August 2017

title

Exon deletion pattern in duchene muscular dystrophy in north west of iran (English)

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8 August 2017

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Mohammad Barzegar

1

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8 August 2017

Parinaz Habibi

2

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8 August 2017

Mortaza Bonyady

3

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8 August 2017

Vahideh Topchizadeh

4

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8 August 2017

Shadi Shiva

5

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8 August 2017

publication date

1 January 2015

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Iranian journal of child neurology

8 August 2017

published in

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8 August 2017

volume

9

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8 August 2017

issue

1

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8 August 2017

page(s)

42-48

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Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Experience and strategy for the molecular testing of Duchenne muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Clinical and molecular studies in Duchenne muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation

12 July 2018

1 reference

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Improved diagnosis of Duchenne/Becker muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Population frequencies of inherited neuromuscular diseases—A world survey

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Point mutations in the dystrophin gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322498

Prevalence and incidence of Becker muscular dystrophy

26 September 2018

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12 December 2020

Clinical trial in Duchenne dystrophy. I. The design of the protocol

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12 December 2020

Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians

1 reference

12 December 2020

De novo mutations in sporadic deletional Duchenne muscular dystrophy (DMD) cases

1 reference

12 December 2020

Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophy

1 reference

12 December 2020

Local dystrophin restoration with antisense oligonucleotide PRO051

1 reference

12 December 2020

Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy

1 reference

12 December 2020

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

Becker muscular dystrophy patients with deletions around exon 51; a promising outlook for exon skipping therapy in Duchenne patients

1 reference

12 December 2020

Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

Identifiers

PMC publication ID

4322498

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8 August 2017

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