Your search returned 2 results.

Results
	1.	CLCN1 mutations in Czech patients with myotonia congenita, in silico analysis of novel and known mutations in the human dimeric skeletal muscle chloride channel. [electronic resource] by Skálová, Daniela Zídková, Jana Voháňka, Stanislav Mazanec, Radim Mušová, Zuzana Vondráček, Petr Mrázová, Lenka Kraus, Josef Réblová, Kamila Fajkusová, Lenka Producer: 20141009 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Autosomal recessive limb-girdle muscular dystrophies in the Czech Republic. [electronic resource] by Stehlíková, Kristýna Skálová, Daniela Zídková, Jana Mrázová, Lenka Vondráček, Petr Mazanec, Radim Voháňka, Stanislav Haberlová, Jana Hermanová, Markéta Zámečník, Josef Souček, Ondřej Ošlejšková, Hana Dvořáčková, Nina Solařová, Pavla Fajkusová, Lenka Producer: 20141209 In: BMC neurology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search