Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia (Q36451472)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia |
scientific article |
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Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia (English)
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Sascha Vermeer
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Lihadh Al-Gazali
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Han G Brunner
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Lisenka E L M Vissers
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Erik-Jan Kamsteeg
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Michèl A Willemsen
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Dirk J Lefeber
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Anneke T Vulto-van Silfhout
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Arjan P M de Brouwer
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Willem M R van den Akker
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Corrie E Erasmus
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Janneke H M Schuurs-Hoeijmakers
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Ilse I G M van de Vondervoort
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Bart P van de Warrenburg
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FORGE Canada Consortium
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Bert B A de Vries
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Hans van Bokhoven
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Irene M Janssen
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Ron A Wevers
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Michael T Geraghty
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Salma Ben-Salem
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Susanne T de Bot
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Bonnie Nijhof
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Marinette van der Graaf
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Anna Castells Nobau
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Irene Otte-Höller
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Amanda C Smith
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Peter Humphreys
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Saeed A Al-Yahyaee
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Said Tariq
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Thachillath Pramathan
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Hubertus P H Kremer
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Saskia van der Velde-Visser
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Adinda Diekstra
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Identifiers
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