Characterization and analysis of branched-chain N-acetylglucosaminyl oligosaccharides accumulating in Sandhoff disease tissue. Evidence that biantennary bisected oligosaccharide si... von Warner, T G, deKremer, R D, Sjoberg, E R, Mock, A K

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Sandhoff disease in Argentina : high frequency of a splice site mutation in the HEXB gene and correlation between enzyme and DNA-based tests for heterozygote detection von KLEIMAN, F. E, DODELSON DE KREMER, R, OLLER DE RAMIREZ, A, GRAVEL, R. A, ARGARANA, C. E

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Charaterization and analysis of branched-chain N-acetylglucosaminyl oligosaccharides accumulating in Sandhoff disease tissue: evidence that biantennary bisected oligosaccharide sid... von WARNER, T. G, DEKREMER, R. D, SJOBERG, E. R, MOCK, A. K

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Diagnosis and characterization of GM 2 gangliosidosis type II (sandhoff disease) by analysis of the accumulating N-acetyl-glucosaminyl oligosaccharides with high performance liquid... von Warner, Thomas G., De Kremer, Raquel D., Applegarth, Derek, Mock, Amy K.

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Mucopolysaccharidosis type VII (β-glucuronidase deficiency): A chronic variant with an oligosymptomatic severe skeletal dysplasia von de Kremer, Raquel D., Givogri, Irene, Argaraña, Carlos E., Hliba, Ernesto, Conci, Rene, Boldini, Catalina D., Capra, Ana P.

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