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2012 | 1 |
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Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.
Am J Hum Genet. 2012 Dec 7;91(6):1073-81. doi: 10.1016/j.ajhg.2012.10.017. Epub 2012 Nov 21.
Am J Hum Genet. 2012.
PMID: 23176823
Free PMC article.
A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy.
Al-Yahyaee S, Al-Gazali LI, De Jonghe P, Al-Barwany H, Al-Kindi M, De Vriendt E, Chand P, Koul R, Jacob PC, Gururaj A, Sztriha L, Parrado A, Van Broeckhoven C, Bayoumi RA.
Al-Yahyaee S, et al.
Neurology. 2006 Apr 25;66(8):1230-4. doi: 10.1212/01.wnl.0000208501.52849.dd.
Neurology. 2006.
PMID: 16636240
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