Yoshihiro Taura

Identification of RCC1–LCK as a novel fusion gene in pediatric erythroid sarcoma

Motohiro Kato, T. Imamura, E. Konishi, 2022, Pediatric blood & cancer.

Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants

K. Kosaki, T. Takenouchi, T. Chiyonobu, 2021, Human Genome Variation.

Complex hereditary spastic paraplegia associated with episodic visual loss caused by ACO2 variants

K. Kosaki, T. Takenouchi, S. Kosugi, 2021, Human genome variation.

Myosin Va, a Novel Interaction Partner of STXBP1, Is Required to Transport Syntaxin1A to the Plasma Membrane

K. Itoh, T. Chiyonobu, T. Iehara, 2023, Neuroscience.

Leigh-like syndrome with progressive cerebellar atrophy caused by novel HIBCH variants

T. Chiyonobu, K. Isoda, Takahiro Hayashi, 2023, Human genome variation.

Impaired neuronal activity and differential gene expression in STXBP1 encephalopathy patient iPSC-derived GABAergic neurons.

Mami Shibata, H. Okano, M. Morimoto, 2021, Human molecular genetics.