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Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts.

Shintaro Okada, M. Lois Veath, Jean-Pierre Leroy, J S O′Brien
PubMed

Data up to Jan 2025

Published1971
Citations81
References6
Fields
BiologyGeneticsMolecular biologyBiochemistry

Total Citations Per Year

Abstract

References (6)

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

1951 • 319,299 citations

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

1969 • 707 citations

[Tay-Sachs disease].

1973 • 390 citations

Variation of β‐N‐acetylhexosaminidase‐pattern in Tay‐Sachs disease

1969 • 258 citations

Mutant Enzymatic and Cytological Phenotypes in Cultured Human Fibroblasts

1967 • 240 citations

FIVE GANGLIOSIDOSES

1969 • 46 citations

Cited By (0)

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Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts. (1971) – PubMed | Metascience Observatory Explorer