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Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome.
Kerkeni, Nesrine; Kharrat, Maher; Maazoul, Faouzi; Boudabous, Hela; M'rad, Ridha; Trabelsi, Mediha.
Affiliation
  • Kerkeni N; University of Tunis El Manar, Faculty of Medicine of Tunis, Laboratory of Human Genetics LR99ES10, Tunis, Tunisia.
  • Kharrat M; University of Tunis El Manar, Faculty of Medicine of Tunis, Laboratory of Human Genetics LR99ES10, Tunis, Tunisia.
  • Maazoul F; University of Tunis El Manar, Faculty of Medicine of Tunis, Laboratory of Human Genetics LR99ES10, Tunis, Tunisia.
  • Boudabous H; Department of Congenital and Hereditary Diseases, Charles Nicolle Hospital, Tunis, Tunisia.
  • M'rad R; Department of Paediatrics, Rabta Hospital, Tunis, Tunisia.
  • Trabelsi M; University of Tunis El Manar, Faculty of Medicine of Tunis, Laboratory of Human Genetics LR99ES10, Tunis, Tunisia.
J Clin Neurol ; 18(2): 214-222, 2022 Mar.
Article in En | MEDLINE | ID: mdl-35196747
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Neurol Year: 2022 Document type: Article Affiliation country: Túnez Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Neurol Year: 2022 Document type: Article Affiliation country: Túnez Country of publication: