Revision history of "NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP)." (Q37589555)

Jump to navigation Jump to search

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.

17 May 2022

15 November 2021

4 October 2021

23 July 2021

30 April 2021

29 April 2021

3 July 2020

3 April 2019

23 March 2019

11 October 2018

11 September 2018

18 March 2018

21 August 2017