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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A. Sinclair | J. Christodoulou | T. Stojkovic | P. Touraine | S. Quijano-roy | Rocio Rius | D. Thorburn | E. Tucker | J. van den Bergen | S. Jaillard | K. Ayers | Gorjana Robevska | Chloe A Hanna | P. Lamont | J. Dupont | Lurdes Sampaio | A. Isapof | S. Vuillaumier‐Barrot | K. Bell | André M Travessa | S. Whalen | J. Dulon | Andrea Simpson | André M. Travessa