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Q42728041-DB1C8CBC-AFB6-423A-9CAD-36161602A596
Q42728041-DB1C8CBC-AFB6-423A-9CAD-36161602A596
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http://www.wikidata.org/entity/statement/Q42728041-DB1C8CBC-AFB6-423A-9CAD-36161602A596
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.
P2860
Q42728041-DB1C8CBC-AFB6-423A-9CAD-36161602A596
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42728041-DB1C8CBC-AFB6-423A-9CAD-36161602A596
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wasDerivedFrom
2c711f3f237f12d2a20464fab480142641bda01d
P2860
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series