A novel missense KCNJ2 gene mutation associated with andersen tawil syndrome
Küçük Resim Yok
Tarih
2019
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Nature Publishing Group
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
[Abstract Not Available]
Açıklama
Conference: 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
Anahtar Kelimeler
Andersen Tawil Syndrome, Missense, KCNJ2
Kaynak
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)
WoS Q Değeri
Q2
Scopus Q Değeri
Cilt
27
Sayı
Supplement: 1
Künye
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.
