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Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing.
Int J Mol Med. 2001 Oct;8(4):461-8.
Int J Mol Med. 2001.
PMID: 11562788
Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs.
Seeman P, Mazanec R, Zidar J, Hrusáková S, Ctvrtecková M, Rautenstrauss B.
Seeman P, et al. Among authors: ctvrteckova m.
Int J Mol Med. 2000 Oct;6(4):421-6. doi: 10.3892/ijmm.6.4.421.
Int J Mol Med. 2000.
PMID: 10998431
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