A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
Autor: | Oh, Se-Kyung1, Baek, Jeong-In2, Weigand, Karl M3, Venselaar, Hanka4, Swarts, Herman G P3, Park, Seong-Hyun5, Hashim Raza, Muhammad6, Jung, Da Jung7, Choi, Soo-Young8, Lee, Sang-Heun7, Friedrich, Thomas9, Vriend, Gert4, Koenderink, Jan B3, Kim, Un-Kyung10, Lee, Kyu-Yup7 |
---|---|
Zdroj: | European Journal of Human Genetics. May2015, Vol. 23 Issue 5, p639-645. 7p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |