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	1.	Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients. [electronic resource] by Marzouki, Naima Benomar, Ali Yahyaoui, Mohamed Birouk, Nezha Elouazzani, Mohamed Chkili, Taib Benlemlih, Mohamed Producer: 20050810 In: European journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Exome sequencing can improve diagnosis and alter patient management. [electronic resource] by Dixon-Salazar, Tracy J Silhavy, Jennifer L Udpa, Nitin Schroth, Jana Bielas, Stephanie Schaffer, Ashleigh E Olvera, Jesus Bafna, Vineet Zaki, Maha S Abdel-Salam, Ghada H Mansour, Lobna A Selim, Laila Abdel-Hadi, Sawsan Marzouki, Naima Ben-Omran, Tawfeg Al-Saana, Nouriya A Sonmez, F Müjgan Celep, Figen Azam, Matloob Hill, Kiley J Collazo, Adrienne Fenstermaker, Ali G Novarino, Gaia Akizu, Naiara Garimella, Kiran V Sougnez, Carrie Russ, Carsten Gabriel, Stacey B Gleeson, Joseph G Producer: 20121019 In: Science translational medicine vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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