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Q47099811-22CB4E2E-FBE4-48CE-B6E4-FF6174EC8712
Q47099811-22CB4E2E-FBE4-48CE-B6E4-FF6174EC8712
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http://www.wikidata.org/entity/statement/Q47099811-22CB4E2E-FBE4-48CE-B6E4-FF6174EC8712
Genomic copy number variation analysis in multiple system atrophy.
P2860
Q47099811-22CB4E2E-FBE4-48CE-B6E4-FF6174EC8712
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47099811-22CB4E2E-FBE4-48CE-B6E4-FF6174EC8712
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126a6bf909b853bda9ef41bc7bfb5c75203057d3
P2860
A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation.