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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English | 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)
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Naima Marzouki
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Ali Benomar
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Mohamed Yahyaoui
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Nezha Birouk
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Mohamed Elouazzani
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Taib Chkili
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Mohamed Benlemlih
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1 January 2005
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