(Q40137142)

17 September 2017

title

Rett syndrome: North American database (English)

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17 September 2017

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Patrick MacLeod

9

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Alan K. Percy

1

object named as

Alan K Percy

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17 September 2017

8

Daniel G Glaze

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17 September 2017

Jane B Lane

2

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Jerry Childers

3

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Steve Skinner

4

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17 September 2017

Fran Annese

5

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Judy Barrish

6

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Erwin Caeg

7

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17 September 2017

publication date

1 December 2007

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Journal of Child Neurology

17 September 2017

published in

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17 September 2017

volume

22

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issue

12

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17 September 2017

page(s)

1338-1341

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

17 September 2017

cites work

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https://api.crossref.org/works/10.1177%2F0883073807308715

Rett syndrome: model of neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Rett syndrome in Australia: a review of the epidemiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Rett syndrome in Spain: mutation analysis and clinical correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

MECP2 gene mutation analysis in Chinese patients with Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Italian Rett database and biobank.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

21 January 2018

Identifiers

DOI

10.1177/0883073807308715

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17 September 2017

1 reference