(Q51958928)

18 April 2018

title

Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling. (English)

1 reference

18 April 2018

author

Laurent Villard

5

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18 April 2018

author name string

Anne Moncla

1

1 reference

18 April 2018

Arlette Kpebe

2

1 reference

18 April 2018

Chantal Missirian

3

1 reference

18 April 2018

Josette Mancini

4

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18 April 2018

publication date

1 January 2002

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18 April 2018

European Journal of Human Genetics

published in

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18 April 2018

volume

10

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18 April 2018

issue

1

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18 April 2018

page(s)

86-89

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18 April 2018

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200761

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

MECP2 mutation in male patients with non-specific X-linked mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

MECP2 is highly mutated in X-linked mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

MECP2 mutation in non-fatal, non-progressive encephalopathy in a male

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Occurrence of Rett syndrome in boys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Male Rett syndrome variant: application of diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

Two affected boys in a Rett syndrome family: clinical and molecular findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

inferred from DOI database lookup

7 January 2021

based on heuristic

MeCP2 mutations in children with and without the phenotype of Rett syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

inferred from DOI database lookup

7 January 2021

based on heuristic

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200761

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5200761

1 reference

18 April 2018

PubMed ID

11896461

1 reference

18 April 2018