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L. A. Pennacchio
发表
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk
Dilenny M. Gonzalez, Rebecca E. Andersen, Connor J Kenny, 2023, medRxiv.
Genetics of epilepsy : Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
L. A. Pennacchio, 1996 .