A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome

Sözügüzel, Mavi DenizIşık, Fatma BüşraGenç, Nimetullah MeteÇaralan, E. F.Doğru, ZübeyirAkdeniz, CoşkunCangül, Hakan2019-12-302019-12-302019Sözügüzel, M. D., Işık, F. B., Genç, N., Caralan, E. F., Doğru, Z., Akdeniz, C. ... Cangül, H. (2019). A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) içinde (918-918. ss.). Milan, Italy, June 16-19, 2018.1018-48131476-5438https://hdl.handle.net/20.500.12511/4799Conference: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) Location: Milan, ITALY Date: JUN 16-19, 2018[Abstract Not Available]eninfo:eu-repo/semantics/closedAccessAndersen Tawil SyndromeMissenseKCNJ2A novel missense KCNJ2 gene mutation associated with andersen tawil syndromeConference Object27Supplement: 1918918Q2