A recurrent mutation inKCNA2as a novel cause of hereditary spastic paraplegia and ataxia

Multilingual Wikipedia

In June 2020 the work A recurrent mutation inKCNA2as a novel cause of hereditary spastic paraplegia and ataxia was on the 800,242nd place in the ranking of the most reliable and popular publications with DOI number in multilingual Wikipedia from readers' point of view (PR-score). If we consider only frequency of appearance of this source in references of Wikipedia articles (F-score), this work was on the 891,020th place in June 2020. From Wikipedians' point of view, "A recurrent mutation inKCNA2as a novel cause of hereditary spastic paraplegia and ataxia" is the 815,758th most reliable publication with DOI number in different language versions of Wikipedia (AR-score).

PR-score:
800,242nd place
900
-500
AR-score:
815,758th place
163
0
F-score:
891,020th place
1
0

English Wikipedia (en)

PR-score:
674,213th place
900
-500
AR-score:
683,082nd place
163
0
F-score:
685,988th place
1
0

BestRef shows popularity and reliability scores for sources in references of Wikipedia articles in different languages. Data extraction based on complex method using Wikimedia dumps. To find the most popular and reliable sources we used information about over 200 million references of Wikipedia articles. More details...