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Authors: Amjad Farooq
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Journal Article

SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency Free

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Adriana P Rebelo and others
Brain, Volume 141, Issue 3, March 2018, Pages 662–672, https://doi.org/10.1093/brain/awx369
Published: 16 January 2018
Journal Article

PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum Get access

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Matthis Synofzik and others
Brain, Volume 137, Issue 1, January 2014, Pages 69–77, https://doi.org/10.1093/brain/awt326
Published: 18 December 2013