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	1.	The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features. [electronic resource] by Leonardis, L Auer-Grumbach, M Papić, L Zidar, J Producer: 20130430 In: European journal of neurology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome. [electronic resource] by Auer-Grumbach, M Fischer, C Papić, L John, E Plecko, B Bittner, R E Bernert, G Pieber, T R Miltenberger, G Schwarz, R Windpassinger, C Grill, F Timmerman, V Speicher, M R Janecke, A R Producer: 20080731 In: Neuropediatrics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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