A neurodegenerative mitochondrial disease phenotype due to biallelic loss-of-function variants in PNPLA8 encoding calcium-independent phospholipase A2γ

Anju Shukla, Russell P. Saneto, Malavika Hebbar, Ghayda Mirzaa, Katta M. Girisha

Research output: Contribution to journal › Article › peer-review

8 Citations (Scopus)

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Medicine & Life Sciences