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	1.	Hemolytic anemia and metabolic acidosis: think about glutathione synthetase deficiency. [electronic resource] by Ben Ameur, Salma Aloulou, Hajer Nasrallah, Fehmi Kamoun, Thouraya Kaabachi, Naziha Hachicha, Mongia Producer: 20150921 In: Fetal and pediatric pathology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Aminoacidopathies and organic acidurias in Tunisia: a retrospective survey over 23 years. [electronic resource] by Hadj-Taieb, Sameh Nasrallah, Fehmi Hammami, Mohamed B Elasmi, Monia Sanhaji, Haifa Moncef, Feki Kaabachi, Naziha Producer: 20120627 In: La Tunisie medicale vol. 90 Availability: No items available. Save to lists Add to cart (remove)
	3.	3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature. [electronic resource] by Kraoua, Ichraf Wiame, Elsa Kraoua, Lilia Nasrallah, Fehmi Benrhouma, Hanen Rouissi, Aida Turki, Ilhem Chaabouni, Habiba Briand, Gilbert Kaabachi, Naziha Van Schaftingen, Emile Gouider-Khouja, Neziha Producer: 20140508 In: Neuropediatrics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	[A novel mutation in PEX 26 gene in Zellweger syndrome: a case report]. [electronic resource] by Ben Turkia, Hadhami Yangui, Mohamed Azzouz, Hatem Ben Chehida, Amal Ben Abelaziz, Rim Abdelmoula, Mohamed Slim Nasrallah, Fehmi Kaabachi, Naziha Wanders, Ronald Tebib, Neji Ben Dridi, Marie Françoise Producer: 20110801 In: La Tunisie medicale vol. 89 Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome. [electronic resource] by Bouyacoub, Yosra Zribi, Hela Azzouz, Hatem Nasrallah, Fehmi Abdelaziz, Rim Ben Kacem, Monia Rekaya, Ben Messaoud, Olfa Romdhane, Lilia Charfeddine, Cherine Bouziri, Mustapha Bouziri, Sonia Tebib, Neji Mokni, Mourad Kaabachi, Naziha Boubaker, Samir Abdelhak, Sonia Producer: 20131029 In: Gene vol. 529 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III. [electronic resource] by Ben Rhouma, Faten Azzouz, Hatem Petit, François M Khelifa, Mariem Ben Chehida, Amel Ben Nasrallah, Fehmi Parisot, Frédéric Lasram, Khaled Kefi, Rym Bouyacoub, Yosra Romdhane, Lilia Baussan, Christiane Kaabachi, Naziha Ben Dridi, Marie-Françoise Tebib, Neji Abdelhak, Sonia Producer: 20140129 In: Molecular biology reports vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)