A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome
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2019Author
Sözügüzel, Mavi DenizIşık, Fatma Büşra
Genç, Nimetullah Mete
Çaralan, E. F.
Doğru, Zübeyir
Akdeniz, Coşkun
Cangül, Hakan
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Sözügüzel, 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.Abstract
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51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)Volume
27Issue
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