Kiyomitsu Nara
1PUBLICATIONS
10CO-AUTHORS
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Publications (1)
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|Apr 16, 2020
Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans.Hideki Mutai, Koichiro Wasano, Yukihide Momozawa
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Frequent Collaborators
1 joint publications
Hideki Mutai
1 joint publications
Koichiro Wasano
1 joint publications
Yoichiro Kamatani
1 joint publications
Fuyuki Miya
1 joint publications
Sawako Masuda
1 joint publications
Noriko Morimoto
1 joint publications
Satoe Takahashi
1 joint publications
Tatsuhiko Tsunoda
1 joint publications
Kazuaki Homma
1 joint publications
Michiaki Kubo
