Whole exome sequencing may be insufficient to cover the causality spectrum of rhabdomyolysis

Josef Finsterer (1) , Sinda Zarrouk-Mahjoub (2)

1 Krankenanstalt Rudolfstiftung
2 LR11IPT05 - Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory

Correspondance

Mots clés: Genotype; Mitochondrial; Pathogenicity; Phenotype; Rhabdomyolysis; Whole exome sequencing; mtDNA

Domaines: Sciences du Vivant [q-bio]

Josef Finsterer, Sinda Zarrouk-Mahjoub. Whole exome sequencing may be insufficient to cover the causality spectrum of rhabdomyolysis. Molecular Genetics and Metabolism Reports, 2018, 17, pp.18. ⟨10.1016/j.ymgmr.2018.08.001⟩. ⟨pasteur-02003296⟩