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

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Published in Hum Mutat on April 01, 2010

Authors

Katherine J Dick1, 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

Author Affiliations

1: Medical Genetics, Clinical Developmental Sciences, St George's University of London, London, UK.

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