(Q36286529)

13 August 2017

1 reference

title

Rett syndrome: model of neurodevelopmental disorders (English)

1 reference

neurodevelopmental disorder

13 August 2017

1 reference

0 references

1

Alan K Percy

1 reference

13 August 2017

Jane B Lane

2

1 reference

13 August 2017

1 September 2005

1 reference

Journal of Child Neurology

13 August 2017

1 reference

13 August 2017

20

1 reference

13 August 2017

9

1 reference

13 August 2017

718-721

1 reference

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

13 August 2017

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

Rett syndrome: Criteria for inclusion and exclusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

Rett variants: a suggested model for inclusion criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

Reduced folate transport to the CNS in female Rett patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200090301

10.1177/08830738050200090301

21 January 2018

Identifiers

DOI

0 references

PubMed ID

16225824

1 reference

PubMed ID

16225824