impact:

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

According to PR-model, A recurrent mutation inKCNA2as a novel cause of hereditary spastic paraplegia and ataxia is ranked 1,488,665th in multilingual Wikipedia, in particular this website is ranked 1,187,591st in English Wikipedia.

#Language
PR-model F-model AR-model
1,488,665th place
1,556,440th place
1,610,629th place
1,187,591st place
1,023,641st place
1,273,537th place