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Aya Yoshida
Aya Yoshida
Nagoya City University
Haploinsufficiency
Medicine
Epilepsy
Hearing loss
Phenotype
2
Papers
1
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0
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An infant case of pseudohypoaldosteronism type1A caused by a novel NR3C2 variant.
2021
Human genome variation
Saki Noda
Kohei Aoyama
Yuto Kondo
Jun Okamura
Atsushi Suzuki
Naoya Yamaguchi
Aya Yoshida
Yoshishige Miyake
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De novo 2q36.3q37.1 deletion encompassing TRIP12 and NPPC yields distinct phenotypes
2020
Human genome variation
Yuto Kondo
Kohei Aoyama
Hisato Suzuki
Ayako Hattori
Ikumi Hori
Koichi Ito
Aya Yoshida
Mari Koroki
Kentaro Ueda
Kenjiro Kosaki
Shinji Saitoh
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