Correction: A novel homozygous CHMP1A variant arising from segmental uniparental disomy causes pontocerebellar hypoplasia type 8

J Hum Genet. 2023 Apr;68(4):299. doi: 10.1038/s10038-023-01125-5.

Masamune Sakamoto^{1

2}, Toshihide Shiiki³, Shuji Matsui³, Nobuhiko Okamoto⁴, Eriko Koshimizu¹, Naomi Tsuchida^{1

5}, Yuri Uchiyama^{1

5}, Kohei Hamanaka¹, Atsushi Fujita¹, Satoko Miyatake^{1

6}, Kazuharu Misawa^{1

7}, Takeshi Mizuguchi¹, Naomichi Matsumoto⁸

¹ Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
² Department of Pediatrics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
³ Department of Pediatrics, Tokyo Children Rehabilitation Hospital, Tokyo, Japan.
⁴ Department of Medical Genetics, Osaka Women's and Children's Hospital, Izumi, Japan.
⁵ Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan.
⁶ Department of Clinical Genetics, Yokohama City University Hospital, Yokohama, Japan.
⁷ Riken Center for Advanced Intelligence Project, Tokyo, Japan.
⁸ Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan. naomat@yokohama-cu.ac.jp.

No abstract available

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