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Q35105917-28CFF4EC-5031-43D6-962C-A775C3DE884D
Q35105917-28CFF4EC-5031-43D6-962C-A775C3DE884D
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Statement
http://www.wikidata.org/entity/statement/Q35105917-28CFF4EC-5031-43D6-962C-A775C3DE884D
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease.
P2860
Q35105917-28CFF4EC-5031-43D6-962C-A775C3DE884D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35105917-28CFF4EC-5031-43D6-962C-A775C3DE884D
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048932c5aa2880b9ead0992351f3b0bea6add289
P2860
CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.