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	1.	HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 8. [electronic resource] by Šafka Brožková, Dana Paulasová Schwabová, Jaroslava Neupauerová, Jana Sabová, Jana Krůtová, Marcela Peřina, Vladimír Trková, Marie Laššuthová, Petra Seeman, Pavel Producer: 20170515 In: Journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Four novel point mutations in the PMP22 gene with phenotypes of HNPP and Dejerine-Sottas neuropathy. [electronic resource] by Brožková, Dana Mazanec, Radim Rychlý, Zdeněk Haberlová, Jana Böhm, Jiří Staněk, Jan Plevová, Pavlína Lisoňová, Jana Sabová, Jana Sakmaryová, Iva Seeman, Pavel Producer: 20111205 In: Muscle & nerve vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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