Presentation Information

[2P-968]Identification of a TCF12 splice site variant in a patient with Kallmann Syndrome

○Erina Suzuki1, Hirohito Shima2, Aki Ueda1, Kazuhiko Nakabayashi3, Keiko Matsubara4, Yoko Kuroki 4,5,6, Junko Kanno2, Maki Fukami1,4 (1. Department of Molecular Endocrinology National Research Institute for Child Health and Development , 2. Department of Pediatrics Tohoku University School of Medicine, 3. Department of Maternal-Fetal Biology, National Center for Child Health and Development, 4. Division of Diversity Research, National Research Institute for Child Health and Development, 5. Department of Genome Medicine National Research Institute for Child Health and Development, 6. Division of Collaborative Research, National Research Institute for Child Health and Development)

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