Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia

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Description scientific article
Author/s

author: Riad Bayoumi  Irene M Janssen  Annette Schenck  Joris A Veltman  Ron A. Wevers  Han G. Brunner  Sascha Vermeer  Jeremy Schwartzentruber  Arjan P M de Brouwer  Dirk J Lefeber  Willem van den Akker  Bart van de Warrenburg  Anneke T Vulto-van Silfhout  Ilse I G M van de Vondervoort  Lihadh Al-Gazali  Martin Lammens  Janneke H M Schuurs-Hoeijmakers  FORGE Canada  Michèl A A P Willemsen  Bert B A de Vries  Corrie E Erasmus  Erik-Jan Kamsteeg  Lisenka Vissers  Hans van Bokhoven  Bassam R. Ali  Christian Gilissen 

Publication date November 21, 2012
Language English
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