Margarita Olympiou
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Explore the profile of Margarita Olympiou including associated specialties, affiliations and a list of published articles.
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2
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32
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Recent Articles
1.
Kyriakoudi S, Sargiannidou I, Kagiava A, Olympiou M, Kleopa K
Hum Mol Genet
. 2017 Mar;
26(9):1622-1633.
PMID: 28334782
Numerous GJB1 gene mutations cause the X-linked form of Charcot-Marie-Tooth disease (CMT1X). GJB1 encodes connexin32 (Cx32), which forms trans-myelin gap junctions in Schwann cells. Most GJB1 mutations result in loss-of-function...
2.
Olympiou M, Sargiannidou I, Markoullis K, Karaiskos C, Kagiava A, Kyriakoudi S, et al.
Acta Neuropathol Commun
. 2016 Sep;
4(1):95.
PMID: 27585976
X-linked Charcot-Marie-Tooth disease (CMT1X) is a common form of inherited neuropathy resulting from different mutations affecting the gap junction (GJ) protein connexin32 (Cx32). A subset of CMT1X patients may additionally...