Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in

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Updated: Jun 27, 2026

Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes
08:56

Modeling Mitochondrial Disease Using Brain Organoids: A Focus on Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes

Published on: October 10, 2025

Sarah Hammond1, Dervla M Connaughton1,2

  • 1Division of Nephrology, Department of Medicine, London Health Sciences Centre, London, Ontario, Canada.

Clinical Genetics
|June 26, 2026
PubMed

Keywords:
TMEM126Bgenetic testingkidney failuremitochondrial complex I deficiencymitochondrial nephropathy

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