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Results: 1-4 |
Results: 4

Authors: Svenson, IK Ashley-Koch, AE Gaskell, PC Riney, TJ Cumming, WJK Kingston, HM Hogan, EL Boustany, RMN Vance, JM Nance, MA Pericak-Vance, MA Marchuk, DA
Citation: Ik. Svenson et al., Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia, AM J HU GEN, 68(5), 2001, pp. 1077-1085

Authors: Hauser, MA Horrigan, SK Salmikangas, P Torian, UM Viles, KD Dancel, R Tim, RW Taivainen, A Bartoloni, L Gilchrist, JM Stajich, JM Gaskell, PC Gilbert, JR Vance, JM Pericak-Vance, MA Carpen, O Westbrook, CA Speer, MC
Citation: Ma. Hauser et al., Myotilin is mutated in limb girdle muscular dystrophy 1A, HUM MOL GEN, 9(14), 2000, pp. 2141-2147

Authors: Rosenberg, CK Pericak-Vance, MA Saunders, AM Gilbert, JR Gaskell, PC Hulette, CM
Citation: Ck. Rosenberg et al., Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutation, ACT NEUROP, 100(2), 2000, pp. 145-152

Authors: Hulette, CM Pericak-Vance, MA Roses, AD Schmechel, DE Yamaoka, LH Gaskell, PC Welsh-Bohmer, KA Crowther, RA Spillantini, MG
Citation: Cm. Hulette et al., Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684, J NE EXP NE, 58(8), 1999, pp. 859-866
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