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	1.	Novel STAMBP mutation and additional findings in an Arabic family. [electronic resource] by Faqeih, Eissa A Bastaki, Laila Rosti, Rasim Ozgur Spencer, Emily G Zada, AbdulAli P Saleh, Mohammad A M Um, Kyongmi Gleeson, Joseph G Producer: 20151214 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. [electronic resource] by Bonnen, Penelope E Yarham, John W Besse, Arnaud Wu, Ping Faqeih, Eissa A Al-Asmari, Ali Mohammad Saleh, Mohammad A M Eyaid, Wafaa Hadeel, Alrukban He, Langping Smith, Frances Yau, Shu Simcox, Eve M Miwa, Satomi Donti, Taraka Abu-Amero, Khaled K Wong, Lee-Jun Craigen, William J Graham, Brett H Scott, Kenneth L McFarland, Robert Taylor, Robert W Producer: 20131105 In: American journal of human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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