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Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
Barkaoui, E; Cherif, W; Tebib, N; Charfeddine, C; Ben Rhouma, F; Azzouz, H; Ben Chehida, A; Monastiri, K; Chemli, J; Amri, F; Ben Turkia, H; Abdelmoula, M S; Kaabachi, N; Abdelhak, S; Ben Dridi, M F.
Affiliation
  • Barkaoui E; Inherited Metabolic Diseases Unit, Pediatric Department, La Rabta Hospital, Tunis, Tunisia.
J Inherit Metab Dis ; 30(6): 989, 2007 Nov.
Article in En | MEDLINE | ID: mdl-18008183
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Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Glycogen Storage Disease Type I / Glucose-6-Phosphatase Type of study: Diagnostic_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: J Inherit Metab Dis Year: 2007 Document type: Article Affiliation country: Túnez
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Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Glycogen Storage Disease Type I / Glucose-6-Phosphatase Type of study: Diagnostic_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: J Inherit Metab Dis Year: 2007 Document type: Article Affiliation country: Túnez