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pro vyhledávání: '"Irina A. Chekmaryeva"'
Autor:
Roman V. Deev, Sergei N. Bardakov, Mikhail O. Mavlikeev, Ivan A. Yakovlev, Zoya R. Umakhanova, Patimat G. Akhmedova, Raisat M. Magomedova, Irina A. Chekmaryeva, Gimat D. Dalgatov, Artur A. Isaev
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
Plectinopathies are orphan diseases caused by PLEC gene mutations. PLEC is encoding the protein plectin, playing a role in linking cytoskeleton components in various tissues. In this study, we describe the clinical case of a 26-year-old patient with
Externí odkaz:
https://doaj.org/article/3104ec04cb774ed689a171829c28065b