@article{dd17618f5e8640b087526ec20ef3b721,
title = "N98S mutation in NEFL gene is dominantly inherited with a phenotype of polyneuropathy and cerebellar atrophy",
keywords = "Axonal loss, Cerebellar atrophy, Charcot-Marie-Tooth disease, Dysmyelination, Myelin, NEFL, Nerve conduction study",
author = "Yi Yang and Gu, {Li Qiang} and Burnette, {William B.} and Jun Li",
note = "Funding Information: This research is supported by grants from NINDS ( R01NS066927 to J.L.) and the National Center for Advancing Translational Sciences ( UL1TR000445 ). Yi Yang is an international exchange student supported by the International Program for PhD Candidates of Sun Yat-Sen University.",
year = "2016",
month = jun,
day = "15",
doi = "10.1016/j.jns.2016.04.007",
language = "English (US)",
volume = "365",
pages = "46--47",
journal = "Journal of the Neurological Sciences",
issn = "0022-510X",
publisher = "Elsevier B.V.",
}