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Molecular confirmation of founder mutation c.-167A>G in Tunisian patients with PMLD disease.
Kammoun Jellouli, Nadege; Salem, Ikhlass Hadj; Ellouz, Emna; Louhichi, Nacim; tlili, Abdelaziz; Kammoun, Fatma; Triki, Chanez; Fakhfakh, Faiza.
Affiliation
  • Kammoun Jellouli N; Laboratoire de Génétique Moléculaire Humaine. Faculté de Médecine de Sfax Université de Sfax, Tunisia. kammounnad@gmail.com
Gene ; 513(2): 233-8, 2013 Jan 25.
Article in En | MEDLINE | ID: mdl-23142375
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Connexins / Founder Effect / Pelizaeus-Merzbacher Disease / Mutation Limits: Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Gene Year: 2013 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Connexins / Founder Effect / Pelizaeus-Merzbacher Disease / Mutation Limits: Female / Humans / Male Country/Region as subject: Africa Language: En Journal: Gene Year: 2013 Document type: Article