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	1.	Emery-Dreifuss muscular dystrophy: a novel mutation in the LMNA gene. [electronic resource] by Lassuthová, Petra Baránková, Lucia Kraus, Josef Maríková, Tat'ána Seeman, Pavel Producer: 20090921 In: Pediatric neurology vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Quantitative multiplex real-time PCR for detection of PLP1 gene duplications in Pelizaeus-Merzbacher patients. [electronic resource] by Mikesová, Emilie Baránková, Lucia Sakmaryová, Iva Tatarková, Iva Seeman, Pavel Producer: 20070618 In: Genetic testing vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutations in the LMNA gene do not cause axonal CMT in Czech patients. [electronic resource] by Lassuthová, Petra Baránková, Lucia Haberlová, Jana Mazanec, Radim Wallace, Andrew Huehne, Kathrin Rautenstrauss, Bernd Seeman, Pavel Producer: 20091215 In: Journal of human genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	L239F founder mutation in GDAP1 is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype. [electronic resource] by Kabzińska, Dagmara Strugalska-Cynowska, Halina Kostera-Pruszczyk, Anna Ryniewicz, Barbara Posmyk, Renata Midro, Alina Seeman, Pavel Báranková, Lucia Zimoń, Magdalena Baets, Jonathan Timmerman, Vincent Guergueltcheva, Velina Tournev, Ivailo Sarafov, Stayko De Jonghe, Peter Jordanova, Albena Hausmanowa-Petrusewicz, Irena Kochański, Andrzej Producer: 20100924 In: Neurogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)