(Q47577126)

4 February 2018

title

Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome (English)

1 reference

4 February 2018

0 references

1 reference

Inui K

1

1 reference

4 February 2018

Akagi M

2

1 reference

4 February 2018

Ono J

3

1 reference

4 February 2018

Tsukamoto H

4

1 reference

4 February 2018

Shimono K

5

1 reference

4 February 2018

Mano T

6

1 reference

4 February 2018

Imai K

7

1 reference

4 February 2018

Yamada M

8

1 reference

4 February 2018

Muramatsu T

9

1 reference

4 February 2018

Sakai N

10

1 reference

4 February 2018

Okada S

11

1 reference

4 February 2018

publication date

1 July 2001

1 reference

4 February 2018

published in

Brain and Development

1 reference

4 February 2018

volume

23

1 reference

4 February 2018

issue

4

1 reference

4 February 2018

page(s)

212-215

1 reference

4 February 2018

Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Rett syndrome in Sweden.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Rett's syndrome in the west of Scotland

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

MECP2 mutations account for most cases of typical forms of Rett syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

Rett variants: a suggested model for inclusion criteria.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900197-8

7 January 2021

10.1016/S0387-7604(01)00197-8

Identifiers

DOI

1 reference

4 February 2018

1 reference

4 February 2018