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Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM)

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Description scientific article published on 12 May 2020
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author: Sylvie Jaillard  Elena J Tucker 

Publication date May 12, 2020
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