Associated Papers
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.
Sajan SA et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2017
Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry.
Pecina P et al.
Bba Clinical, 2014
Select a paper to view details