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Ken Inoue

4PUBLICATIONS
9CO-AUTHORS
Developmental genetics (incl. sex determination)Psychology of ageingNeurology and neuromuscular diseases
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Publications (4)

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|Apr 23, 2026
Pontocerebellar hypoplasia type 9 with a novel combination of compound heterozygous variants in AMPD2.

|Jun 18, 2025
SCN1A gain of function effects in Dravet syndrome: Insights into clinical phenotypes and therapeutic implications.

Yoko Kobayashi Takahashi, Kenshiro Tabata, Shimpei Baba

|Oct 28, 2024
<i>WDR45</i> variants as a major cause for a clinically variable intellectual disability syndrome from early infancy in females.

Chihiro Abe-Hatano, Ken Inoue, Eri Takeshita

|Jul 01, 2024
A novel heterozygous TMEM63A variant in a familial case with early onset nystagmus, severe hypomyelination, and a favorable adult prognosis.

Shota Yoneno, Kaoru Yamamoto, Kenshiro Tabata

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Frequent Collaborators

2 joint publications

Hirotomo Saitsu

1 joint publications

Chihiro Abe-Hatano

1 joint publications

Yosuke Kawai

1 joint publications

Yu-Ichi Goto

1 joint publications

Yoko Kobayashi Takahashi

1 joint publications

Shimpei Baba

1 joint publications

Takashi Saito

1 joint publications

Shinichi Hirose

1 joint publications

Naomichi Matsumoto

Frequent Collaborators

2 joint publications

Hirotomo Saitsu

1 joint publications

Chihiro Abe-Hatano

1 joint publications

Yosuke Kawai

1 joint publications

Yu-Ichi Goto

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