Novel ITPA variants identified by whole genome sequencing and RNA sequencing

Approximately 80% of rare diseases have a genetic cause, and an accurate genetic diagnosis is necessary for disease management, prognosis prediction, and genetic counseling. Whole-exome sequencing (WES) is a cost-effective approach for exploring the genetic cause, but several cases often remain undi...

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Veröffentlicht in:Journal of human genetics 2023-09, Vol.68 (9), p.649-652
Hauptverfasser: Omichi, Nanako, Kishita, Yoshihito, Nakama, Mina, Sasai, Hideo, Terazawa, Atsushi, Kobayashi, Emiko, Fushimi, Takuya, Sugiyama, Yohei, Ichimoto, Keiko, Nitta, Kazuhiro R, Yatsuka, Yukiko, Ohtake, Akira, Murayama, Kei, Okazaki, Yasushi
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Sprache:eng
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