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INSIGHTS INTO THE CONTRIBUTION OF RARE NON-CODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING

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dc.contributor.author안준용-
dc.date.accessioned2022-04-08T21:35:31Z-
dc.date.available2022-04-08T21:35:31Z-
dc.date.created2022-04-08-
dc.date.issued2019-10-
dc.identifier.issn0924-977X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/139677-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.titleINSIGHTS INTO THE CONTRIBUTION OF RARE NON-CODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING-
dc.typeArticle-
dc.contributor.affiliatedAuthor안준용-
dc.identifier.doihttps://doi.org/10.1016/j.euroneuro.2019.07.073-
dc.identifier.wosid000488216600073-
dc.identifier.bibliographicCitationEUROPEAN NEUROPSYCHOPHARMACOLOGY, v.29, pp.36 - 36-
dc.relation.isPartOfEUROPEAN NEUROPSYCHOPHARMACOLOGY-
dc.citation.titleEUROPEAN NEUROPSYCHOPHARMACOLOGY-
dc.citation.volume29-
dc.citation.startPage36-
dc.citation.endPage36-
dc.type.rimsART-
dc.type.docTypeMeeting Abstract-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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