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Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

  1. TitleMutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies
    Author Resko Peter
    Co-authors Radvánszky Ján 1982- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV

    Odnogová Z.

    Baldovič Marián

    Minárik G.

    Poláková Helena SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV

    Pálffy Roland

    Kádaši Ľudevít 1952- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV    ORCID

    Source document General Physiology and Biophysics. Vol. 30, (2011), p. 379-388
    Languageeng - English
    Document kindrozpis článkov z periodík (rbx)
    CitationsADOUKONOU, Thierry Armel - VALLAT, Jean Michel - MATHIS, Stéphane. Charcot-marie-tooth type I disease (CMT-1). In African Journal of Neurological Sciences. ISSN 10158618, 2015-07-11, 34, 1, pp.
    ASADCHUK, T. V. - RUMIANTSEVA, N. V. - NAUMCHIK, I. V. - LIKHACHEV, S. A. - PLESHKO, I. V. - SHALKEVICH, L. V. - JEVNERONOK, I. V. - KACHAN, J. P. Molecular genetic diagnosis and clinical features of hereditary neuropathy with liability to pressure palsies in Belarusian patients. In Zhurnal Nevrologii i Psihiatrii imeni S.S. Korsakova. ISSN 19977298, 2016-01-01, 2016, 1, pp. 64-69.
    CategoryADDA - Scientific papers in domestic journals registered in Current Contents Connect with IF (impacted)
    Category of document (from 2022)V3 - Vedecký výstup publikačnej činnosti z časopisu
    Type of documentčlánok
    Year2011
    article

    article

    rokCCIFIF Q (best)JCR Av Jour IF PercSJRSJR Q (best)CiteScore
    A
    rok vydaniarok metrikyIFIF Q (best)SJRSJR Q (best)
    201120101.146Q40.400Q2
Number of the records: 1  

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