Biochemical and clinical profiles of 52 Tunisian patients affected by Zellweger syndrome

Background: Zellweger syndrome (ZS) is a peroxisome biogenesis disorder attributed to a mutation of the PEX genes family. The incidence of this disease in Africa and the Arab world remains unknown. This contribution is aimed at describing the clinical phenotype and biochemical features in Tunisian p...

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Prif Awduron: Fahmi Nasrallah (Awdur), Wiem Zidi (Awdur), Moncef Feki (Awdur), Samia Kacem (Awdur), Neji Tebib (Awdur), Naziha Kaabachi (Awdur)
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Cyhoeddwyd: Elsevier, 2017-12-01T00:00:00Z.
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