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Comment
. 2018 Sep 1;141(9):e66.
doi: 10.1093/brain/awy184.

A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy

Marina L Kennerson  1   2   3 , Alastair C Corbett  2   4 , Melina Ellis  1 , Gonzalo Perez-Siles  1   2 , Garth A Nicholson  1   2   3
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Comment

A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy

Marina L Kennerson et al. Brain. .
No abstract available

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  • MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
    Ylikallio E, Woldegebriel R, Tumiati M, Isohanni P, Ryan MM, Stark Z, Walsh M, Sawyer SL, Bell KM, Oshlack A, Lockhart PJ, Shcherbii M, Estrada-Cuzcano A, Atkinson D, Hartley T, Tetreault M, Cuppen I, van der Pol WL, Candayan A, Battaloglu E, Parman Y, van Gassen KLI, van den Boogaard MH, Boycott KM, Kauppi L, Jordanova A, Lönnqvist T, Tyynismaa H. Ylikallio E, et al. Brain. 2017 Aug 1;140(8):2093-2103. doi: 10.1093/brain/awx138. Brain. 2017. PMID: 28633435

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