𝔖 Bobbio Scriptorium
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A benign deficiency of type B β-galactosidase in human liver

✍ Scribed by P.S.J. Cheetham; N.B. Dance; D. Robinson


Book ID
115822166
Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
584 KB
Volume
83
Category
Article
ISSN
0009-8981

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The uptake and catabolism of [3H-ceramide]-GM1 was followed in living fibroblasts from patient with different forms of beta-galactosidase deficiency. Gangliosides are identified according to the nomenclature of Svennerholm (1963). A total inability to metabolize the ingested substrate was found in i