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Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Research Abstract Details 

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  • Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Abstract Text:

    isabelle martinIsabelle Martin,julie gauthierJulie Gauthier,marcello d'amelioMarcello D'Amelio,sylviane Sylviane ,patrick vourc'hPatrick Vourc'h,guy a rouleauGuy A Rouleau,antonio m persicoAntonio M Persico,christian r andresChristian R Andres,isabelle martinIsabelle Martin,julie gauthierJulie Gauthier,marcello d'amelioMarcello D'Amelio,sylviane Sylviane ,patrick vourc'hPatrick Vourc'h,guy a rouleauGuy A Rouleau,antonio m persicoAntonio M Persico,christian r andresChristian R Andres,

    Autistic disorder is a neurodevelopmental disorder where genetic factors play an important role. We previously described an association between a subgroup of French autistic patients and an allele of a non-synonymous single nucleotide polymorphism (nsSNP: OMGP62 G>A or rs11080149) in the gene coding for the oligodendrocyte and myelin glycoprotein (OMG), located at 7Mb from the marker D17S250, linked to autism in two independent genome scan studies. We report a study on 431 families with 1 affected child from different origins: French Canada (n=262), Italy (n=123) and United States (n=46). We analyzed the transmission of the rs11080149 alleles from parents to their affected children. There was a preferential transmission of the G allele from parents to affected children (p=0.0017) in the overall sample. Paternal and maternal transmission rates were both skewed. Taking into account our previous results obtained in a French group of patients, where we observed an association with allele A, a direct role of this polymorphism is improbable in autism. The associations observed in Japanese and French patients, the linkage studies and the present work speak in favor of the existence of a susceptibility gene for autism in the NF1 locus.

    Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Publishing Authors By Initials

    i martinI Martin,j gauthierJ Gauthier,m d'amelioM D'Amelio,s S ,p vourc'hP Vourc'h,ga rouleauGA Rouleau,am persicoAM Persico,cr andresCR Andres,i martinI Martin,j gauthierJ Gauthier,m d'amelioM D'Amelio,s S ,p vourc'hP Vourc'h,ga rouleauGA Rouleau,am persicoAM Persico,cr andresCR Andres,

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    Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Neuroscience research

    VOLUME: 59

    Page Numbers: 426-30

    Journal Abbreviation: Neurosci. Res.

    ISSN: 0168-0102

    DAY: 19

    MONTH: 08

    YEAR: 2007

    Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Information

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    LANGUAGE: eng

    NlmUniqueID: 8500749

    Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband. Keywords Mesh Terms:

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    Grant and Affiliation Information for Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.

    AFFILIATION: INSERM, U619, Université François-Rabelais de Tours, CHRU de Tours, Faculté de Médecine, 10 Boulevard Tonnellé, BP3223, 37032, Tours Cedex, France.

    Country: Ireland

    Ireland Research PublicationIreland Research Publication

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    MEDLINETA: Neurosci Res

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