A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report

Overview of attention for article published in Frontiers in Pediatrics, November 2023

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New Research: A novel homozygous splice donor variant in the LRPPRC gene causing Leigh syndrome with epilepsy, a French-Canadian disorder in a Saudi family: case report: Background The mitochondria are a cellular power house. Tissues are… https://t.co/5yv

10 Dec 2023

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