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23. Genetic anticipation in a large family with pure autosomal dominant hereditary spastic paraplegia. Thurmon TF; He C; Haskell C; Thorpe P; Thurmon SG; Rosen DR Am J Med Genet; 1999 Apr; 83(5):392-6. PubMed ID: 10232750 [TBL] [Abstract][Full Text] [Related]
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28. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Hazan J; Lamy C; Melki J; Munnich A; de Recondo J; Weissenbach J Nat Genet; 1993 Oct; 5(2):163-7. PubMed ID: 8252041 [TBL] [Abstract][Full Text] [Related]
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32. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. Olmez A; Uyanik G; Ozgül RK; Gross C; Cirak S; Elibol B; Anlar B; Winner B; Hehr U; Topaloglu H; Winkler J Neuropediatrics; 2006 Apr; 37(2):59-66. PubMed ID: 16773502 [TBL] [Abstract][Full Text] [Related]
35. [A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus callosum]. Tomiyasu H; Hayashi R; Watanabe R; Honda M; Yoshii F Rinsho Shinkeigaku; 1998 May; 38(5):435-9. PubMed ID: 9805990 [TBL] [Abstract][Full Text] [Related]
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