MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression (Q28593334)

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MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
scientific journal article

    Statements

    MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression (English)
    1 reference
    Kirill Makedonski
    1 reference
    Liron Abuhatzira
    1 reference
    Yotam Kaufman
    1 reference
    Aharon Razin
    1 reference
    Ruth Shemer
    1 reference
    15 April 2005
    1 reference
    14
    1 reference
    8
    1 reference
    1049–1058
    1 reference

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