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SOD1 Missense Mutation in a Korean Family with ALS: Clinical Characteristics of Patients with F20C Mutation

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dc.contributor.author김희태-
dc.date.accessioned2021-08-04T04:21:35Z-
dc.date.available2021-08-04T04:21:35Z-
dc.date.issued20051006-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/71778-
dc.description.abstractFamilial ALS (FALS), clinically indistinguishable from sporadic ALS, is mostly expressed as an age-dependent autosomal dominant trait and the disease severity, in terms of the initial sign, the age at onset and disease duration, is diverse between families.-
dc.titleSOD1 Missense Mutation in a Korean Family with ALS: Clinical Characteristics of Patients with F20C Mutation-
dc.typeConference-
dc.citation.conferenceName대한신경과학회 추계학술대회-
dc.citation.conferencePlace그랜드힐튼서울-
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서울 의과대학 > 서울 신경과학교실 > 2. Conference Papers

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