Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3’ exons of TACSTD1

LIGTENBERG Marjolijn J L; KUIPER Roland P; CHAN Tsun Leung; CHAN Tsun Leung; GOOSSENS Monique; HEBEDA Konnie M; VOORENDT Marsha; LEE Tracy Y H; BODMER Danielle; HOENSELAAR Eveline; HENDRIKS-CORNELISSEN S. J B; TSUI Wai Yin; KONG Chi Kwan; BRUNNER Han G; VAN KESSEL Ad Geurts; YUEN Siu Tsan; YUEN Siu Tsan; VAN KRIEKEN J Han J M; LEUNG Suet Yi; LEUNG Suet Yi; HOOGERBRUGGE Nicoline

Art

J-GLOBAL ID：200902294425544042 Reference number：09A0075894

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3’ exons of TACSTD1

リンチ症候群家系でのMSH2の遺伝性の体細胞メチル化による不活化はTACSTD1の3′側に位置するエキソンの欠失が原因である

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Material：
Volume： 41 Issue： 1 Page： 112-117 Publication year： Jan. 2009
JST Material Number： W0430A ISSN： 1061-4036 Document type： Article
Article type：原著論文 Country of issue： United States (USA) Language： ENGLISH (EN)

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Genetic variation , Gene expression

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