Revision history of "Genetic-molecular characterisation of patients with hereditary retina dystrophy of the Basque Country." (Q3139753)

23 March 2024

• curprev 10:0610:06, 23 March 2024‎ DG Regio talk contribs‎ 68,127 bytes +288‎ ‎Added qualifier: readability score (P590521): 0.2552387515242115

20 December 2023

• curprev 16:2716:27, 20 December 2023‎ DG Regio talk contribs‎ 67,839 bytes +7‎ ‎Changed an Item

12 June 2023

• curprev 14:1614:16, 12 June 2023‎ DG Regio talk contribs‎ 67,832 bytes +540‎ ‎Changed an Item

10 June 2023

• curprev 06:4106:41, 10 June 2023‎ Admin talk contribs‎ 67,292 bytes +437‎ BatchIngestion

17 August 2022

• curprev 19:4819:48, 17 August 2022‎ DG Regio talk contribs‎ 66,855 bytes +45,196‎ ‎Changed label, description and/or aliases in el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl, nl, fr, de, it, es, and other parts: Adding translations: el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl,

16 January 2022

• curprev 10:5810:58, 16 January 2022‎ DG Regio talk contribs‎ 21,659 bytes +2,330‎ ‎Changed label, description and/or aliases in it, and other parts: Adding Italian translations

17 December 2021

• curprev 10:1710:17, 17 December 2021‎ DG Regio talk contribs‎ 19,329 bytes +2,314‎ ‎Changed label, description and/or aliases in nl, and other parts: Adding Dutch translations

9 December 2021

• curprev 07:1607:16, 9 December 2021‎ DG Regio talk contribs‎ 17,015 bytes +2,407‎ ‎Changed label, description and/or aliases in de, and other parts: Adding German translations

2 December 2021

• curprev 11:5211:52, 2 December 2021‎ DG Regio talk contribs‎ 14,608 bytes +2,319‎ ‎Created claim: summary (P836): La rétinose pigmentaire (RP) comprend un groupe de maladies héréditaires de la rétine (IRD) associées à un dysfonctionnement progressif des bâtons ou des cônes, ce qui entraîne une perte de vision. Il y a une grande hétérogénéité génétique au sein des IRD avec plus de 250 gènes identifiés, ce qui a entravé leur caractérisation génétique-moléculaire, de sorte que les techniques de séquençage de masse révolutionnent le processus de diagnostic, bie...
• curprev 11:5211:52, 2 December 2021‎ DG Regio talk contribs‎ 12,289 bytes +181‎ ‎Changed label, description and/or aliases in fr: translated_label

12 October 2021

• curprev 13:0113:01, 12 October 2021‎ DG Regio talk contribs‎ 12,108 bytes +162‎ ‎Changed label, description and/or aliases in en: translated_label
• curprev 13:0113:01, 12 October 2021‎ DG Regio talk contribs‎ 11,946 bytes +2,072‎ ‎Created claim: summary (P836): Pigment retinosis (RP) includes a group of hereditary retina diseases (IRD) associated with progressive dysfunction of the sticks or cones, which leads to vision loss. There is a great genetic heterogeneity within IRDs with more than 250 genes identified, which has been hampering their genetic-molecular characterisation, so mass sequencing techniques are revolutionising the diagnostic process, although the genetic cause of 35 % of IRD cases is s...

10 October 2021

• curprev 13:0313:03, 10 October 2021‎ DG Regio talk contribs‎ 9,874 bytes +433‎ ‎Changed an Item: Edited by the materialized bot - inferring region from the coordinates

9 October 2021

• curprev 09:2809:28, 9 October 2021‎ DG Regio talk contribs‎ 9,441 bytes +499‎ ‎Changed an Item: Edited by the infer coords bot - inferring coordinates from location

7 October 2021

• curprev 23:0923:09, 7 October 2021‎ DG Regio talk contribs‎ 8,942 bytes −10‎ ‎Changed label, description and/or aliases in en
• curprev 23:0923:09, 7 October 2021‎ DG Regio talk contribs‎ 8,952 bytes +8,952‎ ‎Created a new Item