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Q50318604-F95C4254-3D98-4B31-A07D-262E9A6286CB
Q50318604-F95C4254-3D98-4B31-A07D-262E9A6286CB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50318604-F95C4254-3D98-4B31-A07D-262E9A6286CB
Whole-exome sequencing identifies novel variants in PNPT1 causing oxidative phosphorylation defects and severe multisystem disease.
P2888
Q50318604-F95C4254-3D98-4B31-A07D-262E9A6286CB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50318604-F95C4254-3D98-4B31-A07D-262E9A6286CB
rank
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type
BestRank
Statement
P2888
ejhg.2016.128