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Q38569822-BFAB1BD3-1CA2-4E05-A17F-8CA40C93EDDE
Q38569822-BFAB1BD3-1CA2-4E05-A17F-8CA40C93EDDE
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Statement
http://www.wikidata.org/entity/statement/Q38569822-BFAB1BD3-1CA2-4E05-A17F-8CA40C93EDDE
Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing.
P2860
Q38569822-BFAB1BD3-1CA2-4E05-A17F-8CA40C93EDDE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38569822-BFAB1BD3-1CA2-4E05-A17F-8CA40C93EDDE
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wasDerivedFrom
4f73221aeab3ce09a600e8bd070e6c4a040722a8
P2860
New tools for Mendelian disease gene identification: PhenoDB variant analysis module; and GeneMatcher, a web-based tool for linking investigators with an interest in the same gene