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Q35204586-CE0BF503-88FB-4623-AB88-147718DF5568
Q35204586-CE0BF503-88FB-4623-AB88-147718DF5568
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35204586-CE0BF503-88FB-4623-AB88-147718DF5568
Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.
P2860
Q35204586-CE0BF503-88FB-4623-AB88-147718DF5568
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35204586-CE0BF503-88FB-4623-AB88-147718DF5568
rank
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type
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Statement
wasDerivedFrom
660ff4aad841628a3e6d628490dcba2b44136a39
P2860
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin