Rett syndrome: a prototypical neurodevelopmental disorder (Q28255289)

neurodevelopmental disorder

Europe PubMed Central

title

Rett syndrome: a prototypical neurodevelopmental disorder (English)

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main subject

Rett syndrome

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1 reference

2

Huda Y Zoghbi

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Jeffrey L. Neul

object named as

Jeffrey L Neul

series ordinal

1

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language of work or name

English

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publication date

April 2004

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published in

The Neuroscientist

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volume

10

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issue

2

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page(s)

118-28

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cites work

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No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

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Low frequency of MECP2 mutations in mentally retarded males.

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Rett syndrome: clinical manifestations in males with MECP2 mutations

21 January 2018

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Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function

21 January 2018

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Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome

21 January 2018

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In-frame deletion inMECP2 causes mild nonspecific mental retardation

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21 January 2018

Identifiers

DOI

10.1177/1073858403260995

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4717185

Fatcat ID

release_wmcodhv5ozcgdgodyk6mx4lx5a

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wmcodhv5ozcgdgodyk6mx4lx5a

mapped directly with Wikidata item

24 November 2022

based on heuristic

OpenCitations bibliographic resource ID

4717185

1 reference