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44. Familial spastic paraplegia with amyotrophy of the hands. Silver JR Ann Hum Genet; 1966 Jul; 30(1):69-75. PubMed ID: 5964029 [No Abstract] [Full Text] [Related]
46. Strumpell's pure familial spastic paraplegia: case study and review of the literature. Holmes GL; Shaywitz BA J Neurol Neurosurg Psychiatry; 1977 Oct; 40(10):1003-8. PubMed ID: 591968 [TBL] [Abstract][Full Text] [Related]
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56. Dominant transmission of de novo KIF1A motor domain variant underlying pure spastic paraplegia. Ylikallio E; Kim D; Isohanni P; Auranen M; Kim E; Lönnqvist T; Tyynismaa H Eur J Hum Genet; 2015 Oct; 23(10):1427-30. PubMed ID: 25585697 [TBL] [Abstract][Full Text] [Related]
57. Spastic paraplegia, glaucoma and mental retardation--in three siblings. A new genetic syndrome. Heijbel J; Jagell S Hereditas; 1981; 94(2):203-7. PubMed ID: 7298353 [No Abstract] [Full Text] [Related]
58. Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus. Sauter SM; Engel W; Neumann LM; Kunze J; Neesen J Hum Mutat; 2004 Jan; 23(1):98. PubMed ID: 14695538 [TBL] [Abstract][Full Text] [Related]
59. Hereditary spastic paraplegia (a review of two families with eight case reports). Rath RN; Das RK; Panda RK; Santhalia RR J Assoc Physicians India; 1978 Jun; 26(6):535-40. PubMed ID: 721758 [No Abstract] [Full Text] [Related]
60. Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndrome. Neuhäuser G; Wiffler C; Opitz JM Clin Genet; 1976 Mar; 9(3):315-23. PubMed ID: 1261070 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]