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1. Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis.

Author

Zaki, M. S., Selim, L., Mansour, L., Mahmoud, I. G., Fenstermaker, A. G., Gabriel, S. B., and Gleeson, J. G.

Subjects
GENETIC mutation, FAMILIES, NEURODEGENERATION
Abstract

A letter to the editor is presented concerning the fatty acid 2-hydroxylase (FA2H) gene mutation in three Arab families which developed neurodegeneration and hereditary spastic paraparesis.

Published
2015
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