Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia
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author: Jeremy Schwartzentruber, Annette Schenck, Riad Bayoumi, Bassam R. Ali, Christian Gilissen, Joris A Veltman, Martin Lammens, Sascha Vermeer, Lihadh Al-Gazali, Han G. Brunner, Lisenka Vissers, Erik-Jan Kamsteeg, Michèl A A P Willemsen, Dirk J Lefeber, Anneke T Vulto-van Silfhout, Arjan P M de Brouwer, Willem van den Akker, Corrie E Erasmus, Janneke H M Schuurs-Hoeijmakers, Ilse I G M van de Vondervoort, Bart van de Warrenburg, FORGE Canada, Bert B A de Vries, Hans van Bokhoven, Irene M Janssen, Ron A. Wevers
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