(Q35436994)

8 August 2017

title

MECP2 mutation in non-fatal, non-progressive encephalopathy in a male (English)

1 reference

8 August 2017

7

Munnich A

1 reference

8 August 2017

Imessaoudene B

1

1 reference

8 August 2017

Bonnefont JP

2

1 reference

8 August 2017

Royer G

3

1 reference

8 August 2017

Cormier-Daire V

4

1 reference

8 August 2017

Lyonnet S

5

1 reference

8 August 2017

Lyon G

6

1 reference

8 August 2017

Amiel J

8

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 March 2001

1 reference

Journal of Medical Genetics

8 August 2017

number of pages

4

1 reference

based on heuristic

inferred from page(s)

published in

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8 August 2017

volume

38

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8 August 2017

issue

3

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8 August 2017

page(s)

171-174

1 reference

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

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

Angelman syndrome: a review of clinical and genetic aspects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

Rett syndrome in a boy with a 47,XXY karyotype

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

Neonatal encephalopathy in two boys in families with recurrent Rett syndrome.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734835

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

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11238684

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11238684

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.38.3.171

1 reference

8 August 2017

1 reference

8 August 2017

1 reference