Autism spectrum disorder: FRAXE mutation, a rare etiology.

about

Autism spectrum disorder: FRAXE mutation, a rare etiology.

Item

http://www.wikidata.org/entity/Q50305806

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@en

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@nl

type

Item

label

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@en

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@nl

prefLabel

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@en

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@nl

P1476

Autism spectrum disorder: FRAXE mutation, a rare etiology.

@en

P2093

C Café

http://www.w3.org/2001/XMLSchema#string

F Correia

http://www.w3.org/2001/XMLSchema#string

J Almeida

http://www.w3.org/2001/XMLSchema#string

P2860

FRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structure

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

Clinical, cytogenetic, and molecular analysis of three families with FRAXE

FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother.

Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator.

Functional characterization of the AFF (AF4/FMR2) family of RNA-binding proteins: insights into the molecular pathology of FRAXE intellectual disability.

The clinical significance of fragile sites on human chromosomes.

P2888

s10803-014-2185-8

P304

888-892

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S10803-014-2185-8

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Guiomar Oliveira

Susana Mouga

P577

2015-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

25035088

http://www.w3.org/2001/XMLSchema#string

P921

Autism spectrum

autism