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重複遺伝子変異を伴った家族性肥大型心筋症家系における表現型の多様性
http://hdl.handle.net/10470/25843
http://hdl.handle.net/10470/25843816f2a7e-9659-4b57-bf55-b0761157c6ea
名前 / ファイル | ライセンス | アクション |
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KJ00006020027.pdf (969.3 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2010-08-10 | |||||
タイトル | ||||||
タイトル | 重複遺伝子変異を伴った家族性肥大型心筋症家系における表現型の多様性 | |||||
言語 | ||||||
言語 | jpn | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
別タイトル | ||||||
その他のタイトル | Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by Combined Missense Mutations | |||||
著者名 |
新井, 正一
× 新井, 正一× 松岡, 瑠美子× 古谷, 道子× 城尾, 邦隆× 中澤, 誠 |
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著者別名 | ||||||
姓名 | ARAI, Shoichi | |||||
著者別名 | ||||||
姓名 | MATSUOKA, Rumiko | |||||
著者別名 | ||||||
姓名 | FURUTANI, Michiko | |||||
著者別名 | ||||||
姓名 | JOH-O, Kunitaka | |||||
著者別名 | ||||||
姓名 | NAKAZAWA, Makoto | |||||
出版者 | ||||||
出版者 | 東京女子医科大学学会 | |||||
受付日付 | ||||||
日付 | 2010-08-10 | |||||
日付タイプ | Created | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0040-9022 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00161368 | |||||
書誌情報 |
東京女子医科大学雑誌 巻 71, 号 9/10, p. 698-708, 発行日 2001-10-25 |
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著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Although mutations of sarcomere protein genes and mitochondorial DNA (mtDNA) cause familial hypertrophic cardiomyopathy (FHC), the phenotypic expression varies in patients who harbor not only a different disease gene mutation, but also the same one. To investigate phenotypic variability in FHC patients, we analyzed the clinical findings, and performed mutation analysis of the cardiac β-myosin heavy chain (β-MHC) gene, the cardiac troponin T (Tn-T) gene and mtDNA in patients of two FHC families. In all five patients of family A, we found the β-MHC gene mutation (Gly741Trp) and mtDNA mutation (T3394C). In four patients of family B, in addition to the β-MHC gene mutation (Gly741Trp) which we reported previously, the rare polymorphic Tn-T gene mutation (Lys253Arg) was detected in an affected son and unaffected father. Also, nine polymorphic mtDNA missense mutations were found in the affected son and an affected daughter. Especially, six out of nine mutations were found to locate at evolutionarily conservative regions. Coexistence of other genetic abnormalities in β-MHC linked FHC, such as multiple polymorphic mtDNA mutations, may contribute to varying phenotypic expression and explain the heterogeneous behavior of FHC. | |||||
著者所属 | ||||||
東京女子医科大学医学部循環器小児科:国際医療福祉大学保健学部放射線・情報科学科 | ||||||
著者所属 | ||||||
東京女子医科大学医学部循環器小児科 | ||||||
著者所属 | ||||||
東京女子医科大学医学部循環器小児科 | ||||||
著者所属 | ||||||
九州厚生年金病院小児科 | ||||||
著者所属 | ||||||
東京女子医科大学医学部循環器小児科 |