Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

✍ Scribed by 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. Kremer; Bart 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

• Book ID: 118135024
• Publisher: American Society of Human Genetics
• Year: 2012
• Tongue: English
• Weight: 764 KB
• Volume: 91
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1016/j.ajhg.2012.10.017