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Article

A potentially dynamic lysosomal role for the endogenous TRPML proteins.

The Journal of pathology - 1 Oct 2009

Zeevi David A, Frumkin Ayala, Offen-Glasner Vered, Kogot-Levin Aviram, Bach Gideon

Abstract excerpt

Lysosomal storage disorders (LSDs) constitute a diverse group of inherited diseases that result from lysosomal storage of compounds occurring in direct consequence to deficiencies of proteins implicated in proper lysosomal function. Pathology in the LSD mucolipidosis type IV (MLIV), is characterized by lysosomal storage of lipids together with water-soluble materials in cells from every tissue and organ of...

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PMID: 19557826
DOI: 10.1002/path.2587

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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