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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.- Sort by
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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
Research output: Contribution to journal › Article › peer-review