(Q36886749)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

A novel mutation of the ARX gene in a male with nonsyndromic mental retardation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

author name string

Matthew M Troester

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Tamara Trachtenberg

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

publication date

1 June 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

Journal of Child Neurology

2 January 2020

number of pages

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

page(s)

744-748

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

2 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

Human ARX gene: genomic characterization and expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

The phenotypic spectrum of ARX mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

X-linked mental retardation with dystonic movements of the hands

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

Nonsyndromic X-linked mental retardation: where are the missing mutations?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

Screening of the ARX gene in 682 retarded males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

X-linked mental retardation: further lumping, splitting and emerging phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807304000

21 January 2018

Identifiers

DOI

10.1177/0883073807304000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17641262%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference