(Q45882971)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15845029%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

title

Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severity (English)

1 reference

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11 January 2020

4

1 reference

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11 January 2020

Lucio Santoro

6

1 reference

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11 January 2020

Francesco Salvatore

7

1 reference

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11 January 2020

Giulia Frisso

2

1 reference

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11 January 2020

author name string

Carsana A

1

1 reference

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11 January 2020

Tremolaterra MR

3

1 reference

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11 January 2020

Vitale DF

5

1 reference

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11 January 2020

language of work or name

English

0 references

publication date

1 May 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15845029%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

published in

Annals of Human Genetics

1 reference

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11 January 2020

volume

69

1 reference

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11 January 2020

issue

Pt 3

1 reference

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11 January 2020

page(s)

253-259

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15845029%20AND%20SRC:MED&resulttype=core&format=json

Direct detection of exon deletions/duplications in female carriers of and male patients with Duchenne/Becker muscular dystrophy.

11 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1529-8817.2005.00160.X

Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1529-8817.2005.00160.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1529-8817.2005.00160.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1529-8817.2005.00160.X