We only have this paper's title and publication details.
Read it at the sourceThis case study reveals a novel PNPLA2 variant linked to neutral lipid storage disease with myopathy, suggesting a genetic basis for the condition.
No takes yet. Share an insight, caveat, or question.
Thulasimani et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: