Title : Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiency.

Pub. Date : 1989 Nov

PMID : 2512653






1 Functional Relationships(s)
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1 We conclude that the ovine disease is due to a mutation at the genetic locus homologous with that of GM1 gangliosidosis and mucopolysaccharidosis type IVB, suggesting that the primary defect in the ovine disease is a mutation of the beta-galactosidase structural gene. G(M1) Ganglioside galactosidase beta 1 Homo sapiens