(Q43509500)

24 November 2017

title

Adolescent onset cognitive regression and neuropsychiatric symptoms associated with the A140V MECP2 mutation (English)

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24 November 2017

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Hugh J McMillan

2

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Asif Doja

object named as

Asif Doja

series ordinal

3

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author name string

Sunita Venkateswaran

series ordinal

1

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24 November 2017

Peter Humphreys

series ordinal

4

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24 November 2017

publication date

15 November 2013

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Developmental Medicine and Child Neurology

24 November 2017

number of pages

4

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based on heuristic

inferred from page(s)

published in

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24 November 2017

volume

56

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24 November 2017

issue

1

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24 November 2017

page(s)

91-94

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Investigating genotype-phenotype relationships in Rett syndrome using an international data set.

24 November 2017

cites work

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https://api.crossref.org/works/10.1111%2FDMCN.12334

Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

MECP2 is highly mutated in X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Rett syndrome: revised diagnostic criteria and nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Regression in individuals with Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Altered attainment of developmental milestones influences the age of diagnosis of rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

A Rett syndrome MECP2 mutation that causes mental retardation in men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FDMCN.12334

21 January 2018

Identifiers

DOI

10.1111/DMCN.12334

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24 November 2017

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