Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients-Reference-Cited by-同舟云学术

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

Published:2005-01 Issue:1 Volume:48 Page:21-28
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Marzouki Naima,Benomar Ali,Yahyaoui Mohamed,Birouk Nezha,Elouazzani Mohamed,Chkili Taib,Benlemlih Mohamed

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference27 articles.

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2. Friedreich’s disease: V. Variant form with vitamin E deficiency and normal fat absorption;Stumpf;Neurology,1987

3. Friedreich’s ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families;Benhamida;Neurology,1993

4. Isolated vitamin E deficiency in the absence of fat malabsorption familial and sporadic cases: characterization and investigation of causes;Sokol;J. Lab. Clin. Med.,1988

5. Adult-onset spinocerebellar syndrome with idiopathic vitamin E deficiency;Yokota;Ann. Neurol.,1987

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