Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans.

Autor: Mutai, Hideki1 (AUTHOR), Wasano, Koichiro1,2 (AUTHOR), Momozawa, Yukihide3 (AUTHOR), Kamatani, Yoichiro4,5 (AUTHOR), Miya, Fuyuki6,7 (AUTHOR), Masuda, Sawako8 (AUTHOR), Morimoto, Noriko9 (AUTHOR), Nara, Kiyomitsu1 (AUTHOR), Takahashi, Satoe2 (AUTHOR), Tsunoda, Tatsuhiko6,7,10 (AUTHOR), Homma, Kazuaki2,11 (AUTHOR), Kubo, Michiaki12 (AUTHOR), Matsunaga, Tatsuo1,13 (AUTHOR) matsunagatatsuo@kankakuki.go.jp
Zdroj: PLoS Genetics. 4/15/2020, Vol. 16 Issue 4, p1-24. 24p.
Databáze: Academic Search Ultimate
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