Heterozygous FA2H mutations in autism spectrum disorders. - Wikidata - awgldk - TriplyDB

Heterozygous FA2H mutations in autism spectrum disorders.

Heterozygous FA2H mutations in autism spectrum disorders.

http://www.wikidata.org/entity/Q31145342

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Gene co-expression networks shed light into diseases of brain iron accumulation.

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Heterozygous FA2H mutations in autism spectrum disorders.

http://www.wikidata.org/entity/Q31145342

description

2013 nî lūn-bûn

@nan

2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Heterozygous FA2H mutations in autism spectrum disorders.

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Heterozygous FA2H mutations in autism spectrum disorders.

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type

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Heterozygous FA2H mutations in autism spectrum disorders.

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Heterozygous FA2H mutations in autism spectrum disorders.

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Heterozygous FA2H mutations in autism spectrum disorders.

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Heterozygous FA2H mutations in autism spectrum disorders.

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1471-2350-14-124

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BMC Medical Genetics

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Heterozygous FA2H mutations in autism spectrum disorders.

@en

P2093

Anita Beggiato

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Anna Maruani

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Claire S Leblond

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Fréderique Amsellem

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Gudrun Nygren

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Guillaume Huguet

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Hiroko Hama

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I Carina Gillberg

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Isabelle Scheid

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

Mary Coleman

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

P2860

Autism and autism spectrum disorders: diagnostic issues for the coming decade

Functional impact of global rare copy number variation in autism spectrum disorders

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

Patterns and rates of exonic de novo mutations in autism spectrum disorders

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

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

A rare family with Hereditary Spastic Paraplegia Type 35 due to novel FA2H mutations: a case report with literature review.

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Fatty acid 2-Hydroxylation in mammalian sphingolipid biology

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).

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1471-2350-14-124

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124

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scholarly article

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10.1186/1471-2350-14-124

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14

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Christopher Gillberg

Thomas Bourgeron

Catalina Betancur

Henrik Anckarsäter

Richard Delorme

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2013-12-03T00:00:00Z

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259152659

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24299421

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Autism spectrum

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4219428

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