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Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I.
BMC Pediatr. 2020 Jan 29;20(1):41. doi: 10.1186/s12887-020-1912-x.
BMC Pediatr. 2020.
PMID: 31996177
Free PMC article.
Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.
Leslie N, Wang X, Peng Y, Valencia CA, Khuchua Z, Hata J, Witte D, Huang T, Bove KE.
Leslie N, et al.
Hum Pathol. 2016 Mar;49:27-32. doi: 10.1016/j.humpath.2015.09.039. Epub 2015 Oct 28.
Hum Pathol. 2016.
PMID: 26826406
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