Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia

Janneke H.M. Schuurs-Hoeijmakers, Michael T. Geraghty, Erik Jan Kamsteeg, Salma Ben-Salem, Susanne T. De Bot, Bonnie Nijhof, Ilse I.G.M. Van De Vondervoort, Marinette Van Der Graaf, Anna Castells Nobau, Irene Otte-Höller, Sascha Vermeer, Amanda C. Smith, Peter Humphreys, Jeremy Schwartzentruber, Bassam R. Ali, Saeed A. Al-Yahyaee, Said Tariq, Thachillath Pramathan, Riad Bayoumi, Hubertus P.H. KremerBart P. Van De Warrenburg, Willem M.R. Van Den Akker, Christian Gilissen, Joris A. Veltman, Irene M. Janssen, Anneke T. Vulto-Van Silfhout, Saskia Van Der Velde-Visser, Dirk J. Lefeber, Adinda Diekstra, Corrie E. Erasmus, Michèl A. Willemsen, Lisenka E.L.M. Vissers, Martin Lammens, Hans Van Bokhoven, Han G. Brunner, Ron A. Wevers, Annette Schenck, Lihadh Al-Gazali, Bert B.A. De Vries, Arjan P.M. De Brouwer

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

123 Citations (Scopus)

Fingerprint

Dive into the research topics of 'Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia'. Together they form a unique fingerprint.

Medicine & Life Sciences