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Q49991801-E494F511-6E81-41B2-9FB1-84B698E1E4FC
Q49991801-E494F511-6E81-41B2-9FB1-84B698E1E4FC
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Statement
http://www.wikidata.org/entity/statement/Q49991801-E494F511-6E81-41B2-9FB1-84B698E1E4FC
The functional genomics laboratory: functional validation of genetic variants.
P2860
Q49991801-E494F511-6E81-41B2-9FB1-84B698E1E4FC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49991801-E494F511-6E81-41B2-9FB1-84B698E1E4FC
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wasDerivedFrom
adf24dd862a80cbdcae82b28a3aaa85ca8d3911c
P2860
Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease.