DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Schuurs-Hoeijmakers JH, Geraghty MT, Kamsteeg EJ , et al; FORGE Canada Consortium.
Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.
Am J Hum Genet 2012;
91 (6) 1073-1081
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