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	1.	Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients. [electronic resource] by Brožková, Dana Šafka Posádka, Jan Laššuthová, Petra Mazanec, Radim Haberlová, Jana Sišková, Dana Sakmaryová, Iva Neupauerová, Jana Seeman, Pavel Producer: 20140528 In: Molecular medicine reports vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population. [electronic resource] by Marková, Simona Poisson Brožková, Dana Šafka Laššuthová, Petra Mészárosová, Anna Krůtová, Marcela Neupauerová, Jana Rašková, Dagmar Trková, Marie Staněk, David Seeman, Pavel Producer: 20180727 In: Genetic testing and molecular biomarkers vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma. [electronic resource] by Schwabova, Jaroslava Brozkova, Dana Safka Petrak, Borivoj Mojzisova, Mahulena Pavlickova, Klara Haberlova, Jana Mrazkova, Lenka Hedvicakova, Petra Hornofova, Ludmila Kaluzova, Marie Fencl, Filip Krutova, Marcela Zamecnik, Josef Seeman, Pavel Producer: 20140806 In: Journal of neurogenetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2. [electronic resource] by Lassuthova, Petra Rebelo, Adriana P Ravenscroft, Gianina Lamont, Phillipa J Davis, Mark R Manganelli, Fiore Feely, Shawna M Bacon, Chelsea Brožková, Dana Šafka Haberlova, Jana Mazanec, Radim Tao, Feifei Saghira, Cima Abreu, Lisa Courel, Steve Powell, Eric Buglo, Elena Bis, Dana M Baxter, Megan F Ong, Royston W Marns, Lorna Lee, Yi-Chung Bai, Yunhong Isom, Daniel G Barro-Soria, René Chung, Ki W Scherer, Steven S Larsson, H Peter Laing, Nigel G Choi, Byung-Ok Seeman, Pavel Shy, Michael E Santoro, Lucio Zuchner, Stephan Producer: 20181211 In: American journal of human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)