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A first description of ataxia with vitamin E deficiency associated with MT-TG gene mutation.
Maalej, Marwa; Kammoun, Fatma; Kharrat, Marwa; Bouchaala, Wafa; Ammar, Marwa; Mkaouar-Rebai, Emna; Triki, Chahnez; Fakhfakh, Faiza.
Affiliation
  • Maalej M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, Sfax, Tunisia. marwamaalej7@gmail.com.
  • Kammoun F; Unit of Pediatric Neurology research (UR12ES 16), C.H.U. Hedi Chaker, Sfax, Tunisia.
  • Kharrat M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, Sfax, Tunisia.
  • Bouchaala W; Unit of Pediatric Neurology research (UR12ES 16), C.H.U. Hedi Chaker, Sfax, Tunisia.
  • Ammar M; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, Sfax, Tunisia.
  • Mkaouar-Rebai E; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, Sfax, Tunisia.
  • Triki C; Unit of Pediatric Neurology research (UR12ES 16), C.H.U. Hedi Chaker, Sfax, Tunisia.
  • Fakhfakh F; Laboratory of Molecular and Functional Genetics, Faculty of Science of Sfax, Sfax, Tunisia. faiza.fakhfakh02@gmail.com.
Acta Neurol Belg ; 121(6): 1733-1740, 2021 Dec.
Article in En | MEDLINE | ID: mdl-32979145
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / Vitamin E Deficiency / DNA, Mitochondrial / DNA Mutational Analysis / Mutation Type of study: Risk_factors_studies Limits: Adult / Female / Humans Language: En Journal: Acta Neurol Belg Year: 2021 Document type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ataxia / Vitamin E Deficiency / DNA, Mitochondrial / DNA Mutational Analysis / Mutation Type of study: Risk_factors_studies Limits: Adult / Female / Humans Language: En Journal: Acta Neurol Belg Year: 2021 Document type: Article