Parkinsonism Due to <span class='italic'>CSF1R</span> Mutation

David S Lynch; Zane Jaunmuktane; Henry Houlden

doi:10.1017/9781316145050.016

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Print publication year: 2017
Online publication date: July 2017

15 - Parkinsonism Due to CSF1R Mutation

from Section 1 - Parkinsonism

By David S Lynch, Zane Jaunmuktane, Henry Houlden

Kailash P. Bhatia, Institute of Neurology, University College London, Roberto Erro, Maria Stamelou, University of Athens, Greece
Publisher: Cambridge University Press
DOI: https://doi.org/10.1017/9781316145050.016
pp 35-37

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Sundal, C, Fujioka, S, Van Gerpen, JA, et al. Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations. Parkinsonism Relat Disord. 2013;19:869–77.

Guerreiro, R, Kara, E, Le Ber, I et al. Genetic analysis of inherited leukodystrophies: Genotype–phenotype correlations in the CSF1R gene. JAMA Neurol. 2013;70:875–82.

Sundal, C, Van Gerpen, JA, Nicholson, AM et al. MRI characteristics and scoring in HDLS due to CSF1R gene mutations. Neurology. 2012;79:566–74.

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