Absence of KHDC3L mutations in Chinese patients with recurrent and sporadic hydatidiform moles
作者单位：Women's Reproductive Health LaboratoryWomen's Hospital Zhejiang University School of Medicine Hangzhou First People's Hospital Hangzhou hospital of Nanjing Medical University Departments of Human Genetics and dObstetrics and GynecologyMcGill University Health Centre
会议名称：《2013浙江省医学遗传学学术年会》
会议日期：2013年
学科分类：1002[医学-临床医学] 100211[医学-妇产科学] 10[医学]
基 金：supported by the National Natural Science Foundation of China(30973172) the Natural Science Foundation of Zhejiang Province in China(Y2090403) Major Science and Technology Projects of Science and technology Department of Zhejiang Province(2009C14012)
摘 要：To date,two maternal-effect genes have been shown to play causal roles in recurrent hydatidiform moles (RHMs).NLRP7 ,Is a major gene for this condition,codes for a NOD-like receptor,and is mutated in 48