Your search returned 5 results.

Results
	1.	COX6A1 mutation causes axonal hereditary motor and sensory neuropathy - the confirmation of the primary report. [electronic resource] by Laššuthová, P Beharka, R Krůtová, M Neupauerová, J Seeman, P Publication details: Clinical genetics Apr 2016 In: Clinical genetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	High frequency of SH3TC2 mutations in Czech HMSN I patients. [electronic resource] by Laššuthová, P Mazanec, R Vondráček, P Sišková, D Haberlová, J Sabová, J Seeman, P Producer: 20130822 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom. [electronic resource] by Laššuthová, P Brožková, D Šafka Krůtová, M Neupauerová, J Haberlová, J Mazanec, R Dvořáčková, N Goldenberg, Z Seeman, P Producer: 20150827 In: Neurogenetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Monitoring of methylation changes in 9p21 region in patients with myelodysplastic syndromes and acute myeloid leukemia. [electronic resource] by Cechova, H Lassuthova, P Novakova, L Belickova, M Stemberkova, R Jencik, J Stankova, M Hrabakova, P Pegova, K Zizkova, H Cermak, J Producer: 20120717 In: Neoplasma vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B2. [electronic resource] by Laššuthová, P Vill, K Erdem-Ozdamar, S Schröder, J M Topaloglu, H Horvath, R Müller-Felber, W Bansagi, B Schlotter-Weigel, B Gläser, D Neupauerová, J Sedláčková, L Staněk, D Mazanec, R Weis, J Seeman, P Senderek, J Producer: 20191114 In: Clinical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)