[go: up one dir, main page]

Revision history of "Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G)." (Q40678892)

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

26 October 2021

27 September 2021

24 June 2020

23 January 2019

3 December 2018

24 August 2018

5 February 2018

23 September 2017

22 September 2017