Statistics for Aminoacylation-defective bi-allelic mutations in human EPRS1 associated with psychomotor developmental delay, epilepsy, and deafness

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Aminoacylation-defective bi-allelic mutations in human EPRS1 associated with psychomotor developmental delay, epilepsy, and deafness 3

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java.util.UUID:f576f83e-67d9-492f-9d10-34a7ade67a93 20
java.util.UUID:9f8dbc66-84cd-499d-a9ab-e2ae39d25462 12
CGE-103-358.pdf 9
java.util.UUID:f5a70409-cdad-4b2a-849c-2fd638a57378 7

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