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Results: 1-2 |
Results: 2
Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with centralconduction slowing
Authors: Seeman, P Mazanec, R Ctvrteckova, M Smilkova, D
Citation: P. Seeman et al., Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with centralconduction slowing, INT J MOL M, 8(4), 2001, pp. 461-468
Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy withliability to pressure palsies (HNPP): Reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs
Authors: Seeman, P Mazanec, R Zidar, J Hrusakova, S Ctvrteckova, M Rautenstrauss, B
Citation: P. Seeman et al., Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy withliability to pressure palsies (HNPP): Reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs, INT J MOL M, 6(4), 2000, pp. 421-426
Risultati: 1-2 |