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Resolving disease mechanisms through rare mutation discovery: complex disease genetics and somatic mosaicism

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dc.contributor.author하유진-
dc.date.accessioned2026-07-09T19:34:20Z-
dc.date.available2026-07-09T19:34:20Z-
dc.date.issued2026-06-26-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/219031-
dc.titleResolving disease mechanisms through rare mutation discovery: complex disease genetics and somatic mosaicism-
dc.typeConference-
dc.citation.conferenceName2026 한국분자ㆍ세포생물학회 뇌신경발생학분과 정기학술대회-
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서울 자연과학대학 > 서울 생명과학과 > 2. Conference Papers

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