Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

Katherine J. Dick, Matthias Eckhardt, Coro Paisán-Ruiz, Aisha Alkhayat Alshehhi, Christos Proukakis, Naomi A. Sibtain, Helena Maier, Reza Sharifi, Michael A. Patton, Wafa Bashir, Roshan Koul, Sandy Raeburn, Volkmar Gieselmann, Henry Houlden, Andrew H. Crosby

Research output: Contribution to journal › Article › peer-review

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