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

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Description scientific article published on 01 May 2018
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author: Q88432251  Malavika Hebbar  Ghayda Mirzaa  Katta Mohan Girisha 

Publication date May 1, 2018
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