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	1.	Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. [electronic resource] by Heimer, G Eyal, E Zhu, X Ruzzo, E K Marek-Yagel, D Sagiv, Doron Anikster, Y Reznik-Wolf, H Pras, E Oz Levi, D Lancet, D Ben-Zeev, B Nissenkorn, A Producer: 20180628 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum. [electronic resource] by Heimer, G Marek-Yagel, D Eyal, E Barel, O Oz Levi, D Hoffmann, C Ruzzo, E K Ganelin-Cohen, E Lancet, D Pras, E Rechavi, G Nissenkorn, A Anikster, Y Goldstein, D B Ben Zeev, B Producer: 20160627 In: Clinical genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy. [electronic resource] by Hannibal, M C Ruzzo, E K Miller, L R Betz, B Buchan, J G Knutzen, D M Barnett, K Landsverk, M L Brice, A LeGuern, E Bedford, H M Worrall, B B Lovitt, S Appel, S H Andermann, E Bird, T D Chance, P F Producer: 20090601 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. [electronic resource] by Collie, A M B Landsverk, M L Ruzzo, E Mefford, H C Buysse, K Adkins, J R Knutzen, D M Barnett, K Brown, R H Parry, G J Yum, S W Simpson, D A Olney, R K Chinnery, P F Eichler, E E Chance, P F Hannibal, M C Producer: 20101215 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)