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Article

A case of the B1 variant of GM2-gangliosidosis.

Journal of inherited metabolic disease - 1 Jan 1990

Gray R G, Green A, Rabb L, Broadhead D M, Besley G T

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Identifiers

PMID: 2146441
DOI: 10.1007/BF01799373

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patient.Semantic proximity Read ↗

[GM2-Gangliosidosis variant B1 disclosed during adolescence by an isolated multi-systemic involvement of the central and peripheral nervous systems].Semantic proximity Read ↗

GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene abnormalities in seven patients.Semantic proximity Read ↗

Genotypic and phenotypic characterization of Brazilian patients with GM1 gangliosidosis.Semantic proximity Read ↗

Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency.Semantic proximity Read ↗

Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant.Semantic proximity Read ↗

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