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Q55285207-524B05DD-6AF4-4D0B-835E-B529728B441B
Q55285207-524B05DD-6AF4-4D0B-835E-B529728B441B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55285207-524B05DD-6AF4-4D0B-835E-B529728B441B
Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis.
P2860
Q55285207-524B05DD-6AF4-4D0B-835E-B529728B441B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55285207-524B05DD-6AF4-4D0B-835E-B529728B441B
rank
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type
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Statement
wasDerivedFrom
1ffe3899079948ffc4de4c24f751e9a28a947c16
P2860
Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy