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Q52372462-DEE8B81C-BD8E-4F88-BB08-96DAE3C882EB
Q52372462-DEE8B81C-BD8E-4F88-BB08-96DAE3C882EB
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Statement
http://www.wikidata.org/entity/statement/Q52372462-DEE8B81C-BD8E-4F88-BB08-96DAE3C882EB
Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing.
P2860
Q52372462-DEE8B81C-BD8E-4F88-BB08-96DAE3C882EB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52372462-DEE8B81C-BD8E-4F88-BB08-96DAE3C882EB
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wasDerivedFrom
1d2069c574e1460fc2fac574b6aafb61636be841
P2860
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.