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    Heterozygous FA2H mutations in autism spectrum disorders 

    Scheid, Isabelle; Maruani, Anna; Huguet, Guillaume; Leblond, Claire S.; Nygren, Gudrun; Anckarsaeter, Henrik; Beggiato, Anita; Rastam, Maria; Amsellem, Frederique; Gillberg, I. Carina; Elmaleh, Monique; Leboyer, Marion; Gillberg, Christopher; Betancur, Catalina; Coleman, Mary; Hama, Hiroko; Cook, Edwin H.; Bourgeron, Thomas; Delorme, Richard (BioMed Central, 2013-12)
    Background Widespread abnormalities in white matter development are frequently reported in cases of autism spectrum disorders (ASD) and could be involved in the disconnectivity suggested in these disorders. Homozygous ...

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    Author
    Amsellem, Frederique (1)
    Anckarsaeter, Henrik (1)
    Beggiato, Anita (1)
    Betancur, Catalina (1)Bourgeron, Thomas (1)Coleman, Mary (1)Cook, Edwin H. (1)
    Delorme, Richard (1)
    Elmaleh, Monique (1)
    Gillberg, Christopher (1)
    ... View MoreSubject
    Autism; Brain; Gene; Myelin (1)
    ... View MoreDate Issued2013 (1)

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