Mizuno, Seiji
Aichi Developmental Disability Center
2 papers on CoChatORCID 0000-0002-1491-4124
Most cited papers
- Verified
Clinical correlations of mutations affecting six components of the SWI/SNF complex: Detailed description of 21 patients and a review of the literature
Kosho, T., Okamoto, N., Ohashi, H., Tsurusaki, Y., Imai, Y., Hibi‐Ko, Y., Kawame, H., Homma, T., Tanabe, S., Kato, M., et al. (2013) · American Journal of Medical Genetics Part A
Chromatin Remodeling and CancerGenetics and Neurodevelopmental Disorders
Cited by 101
- Verified
Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome
Otsuji, S., Nishio, Y., Tsujita, M., Rio, M., Huber, C., Antón-Plágaro, C., Mizuno, S., Kawano, Y., Miyatake, S., Simon, M., et al. (2023) · Journal of Medical Genetics
Cellular transport and secretionGenomics and Rare Diseases
Cited by 19
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