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Q58122543-3039E0C3-FD9E-4E62-8593-6ED924F041A0
Q58122543-3039E0C3-FD9E-4E62-8593-6ED924F041A0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58122543-3039E0C3-FD9E-4E62-8593-6ED924F041A0
Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause
P2860
Q58122543-3039E0C3-FD9E-4E62-8593-6ED924F041A0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58122543-3039E0C3-FD9E-4E62-8593-6ED924F041A0
rank
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type
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Statement
wasDerivedFrom
eaad9e4fdb01fc23639aff80cb8d5ced02bffab0
P2860
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12