(Q46160928)

English

Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression

scientific article published on 14 July 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

12

object named as

Annick Toutain

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

Delphine Héron

22

object named as

Delphine Héron

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Bernard Echenne

13

object named as

Bernard Echenne

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

author name string

Fatma Daoud

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Nathalie Angeard

2

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Bénédicte Demerre

3

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Itxaso Martie

4

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Rabah Benyaou

5

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

France Leturcq

6

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Mireille Cossée

7

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Nathalie Deburgrave

8

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Yoann Saillour

9

1 reference

Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Sylvie Tuffery

10

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Andoni Urtizberea

11

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Martine Frischman

14

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Michèle Mayer

15

1 reference

Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Isabelle Desguerre

16

1 reference

Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Brigitte Estournet

17

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Christian Réveillère

18

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Penisson-Besnier

19

1 reference

Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Jean Marie Cuisset

20

1 reference

Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Jean Claude Kaplan

21

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

François Rivier

23

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

Jamel Chelly

24

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

publication date

14 July 2009

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

Human Molecular Genetics

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

18

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/19602481

20

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

3779-3794

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

The muscular dystrophies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Cognitive impairment in Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Dystrophin and mutations: one gene, several proteins, multiple phenotypes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Comprehensive detection of genomic duplications and deletions in the DMD gene, by use of multiplex amplifiable probe hybridization

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

The structural and functional diversity of dystrophin

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

A 71-kilodalton protein is a major product of the Duchenne muscular dystrophy gene in brain and other nonmuscle tissues

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Protein truncation test: analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardation.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Syntrophins and dystrobrevins: defining the dystrophin scaffold at synapses

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Pre- and post-synaptic mechanisms regulating the clustering of type A gamma-aminobutyric acid receptors (GABAA receptors).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Different dystrophin-like complexes are expressed in neurons and glia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP320

21 January 2018

Identifiers

10.1093/HMG/DDP320

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/19602481

ResearchGate publication ID

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