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2. GM1 gangliosidosis type 3 with severe jaw-closing impairment. Hirayama M; Kitagawa Y; Yamamoto S; Tokuda A; Mutoh T; Hamano T; Aita T; Kuriyama M J Neurol Sci; 1997 Nov; 152(1):99-101. PubMed ID: 9395131 [TBL] [Abstract][Full Text] [Related]
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19. A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patient. Mosna G; Fattore S; Tubiello G; Brocca S; Trubia M; Gianazza E; Gatti R; Danesino C; Minelli A; Piantanida M Hum Genet; 1992 Nov; 90(3):247-50. PubMed ID: 1487238 [TBL] [Abstract][Full Text] [Related]
20. Comprehensive behavioral and biochemical outcomes of novel murine models of GM1-gangliosidosis and Morquio syndrome type B. Przybilla MJ; Ou L; Tăbăran AF; Jiang X; Sidhu R; Kell PJ; Ory DS; O'Sullivan MG; Whitley CB Mol Genet Metab; 2019 Feb; 126(2):139-150. PubMed ID: 30528226 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]