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

✍ Scribed by Naima Marzouki; Ali Benomar; Mohamed Yahyaoui; Nezha Birouk; Mohamed Elouazzani; Taib Chkili; Mohamed Benlemlih


Book ID
116432768
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
208 KB
Volume
48
Category
Article
ISSN
1769-7212

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