Presentation Information
[P1-01-19]Genetic analysis of family members to evaluate VUS in FLCN detected in a proband diagnosed with Birt-Hogg-Dube syndrome
○Tomomi Oka1, Takeshi Nakajima1,2, Sayaka Honda1, Kiminobu Tanizawa3,4, Masahiro Gotoh5, Makoto Hirata6, Akiko Yoshida1,7, Masako Torishima1,7, Hiromi Murakami1,2, Akira Inaba1, Akari Minamoto1, Sayoko Haruyama1, Kawasaki Hidenori1,7, Masanobu Ogawa1,8, Takahito Wada1,7, Shinji Kosugi1,2,7 (1.Clinical Genetics Unit, Kyoto University Hospital, 2.School of Public Health, Medical Ethics and Medical Genetics, Graduate School of Medicine, Kyoto University, 3.Division of Respiratory Medicine, Center for Respiratory Diseases, National Hospital Organization Kyoto Medical Center, 4.Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, 5.Department of Clinical Genomics, National Cancer Center Research Institute, 6.Department of Genetic Medicine and Services, National Cancer Center Hospital, 7.Department of Genomic Medicine, Graduate School of Medicine, Kyoto University, 8.Ethics Support Unit, Kyoto University Hospital)