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Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal.

Alessandra TorracoReza MaroofianAgnès RötigEnrico Silvio BertiniDaniele GhezziRosalba CarrozzoNazzareno Diodato
Published in: Human mutation (2021)
Keyphrases
  • copy number
  • single cell
  • case report
  • dna methylation