Molecular basis of von Hippel-Lindau syndrome in Chinese patients
Publication in refereed journal


引用次數
替代計量分析
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其它資訊
摘要Background Von Hippel-Lindau (VHL) syndrome is an autosomal dominant familial cancer syndrome predisposing the affected individuals to multiple tumours in various organs. The genetic basis of VHL in Southern Chinese is largely unknown. In this study, we characterized the mutation spectrum of VHL in nine unrelated Southern Chinese families.
著者Siu WK, Ma RCW, Lam CW, Mak CM, Yuen YP, Lo FMI, Chan KW, Lam SF, Ling SC, Tong SF, So WY, Chow CC, Tang MHY, Tam WH, Chan AYW
期刊名稱Chinese Medical Journal
出版年份2011
月份1
日期20
卷號124
期次2
出版社CHINESE MEDICAL ASSOC
頁次237 - 241
國際標準期刊號0366-6999
語言英式英語
關鍵詞Chinese; VHL gene; VHL mutations; von Hippel-Lindau syndrome
Web of Science 學科類別General & Internal Medicine; Medicine, General & Internal; MEDICINE, GENERAL & INTERNAL

上次更新時間 2020-14-09 於 00:42