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 1,921,163^rd in multilingual Wikipedia, in particular this website is ranked 1,514,683^rd in English Wikipedia.

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1,921,163^rd place

1,660,460^th place

2,149,862^nd place

enEnglish

1,514,683^rd place

799,757^th place

1,643,078^th place