Masmoudi, Aida, Department of Embryo-fetopathology, Center of Maternity and Neonatology of Tunis
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Vol 2, No 3 (2015) - Epidemiology and Clinical Research
Familial case study: a recurrent metabolic disease in a Tunisian family
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The Rare Diseases and Orphan Drugs Journal has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under Grant Agreement № 305690: RARE-Bestpractices project: www.rarebestpractices.eu. Sole responsibility lies with the authors and the European Comission is not responsible for any use that may be made of the information contained therein.
