Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients (Q39221489)

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Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients
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    Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients (English)
    Naima Marzouki
    Ali Benomar
    Mohamed Yahyaoui
    Nezha Birouk
    Mohamed Elouazzani
    Taib Chkili
    Mohamed Benlemlih
    1 January 2005
    21-28

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