Correspondence on "Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder" by Cuinat et al.

Sheng Wenchao, Yu Xiaoli, Shu Jianbo, Cai Chunquan

Tianjin Children's Hospital (Tianjin University Children's Hospital), Tianjin, China.

Department of Neurology, Tianjin Children's Hospital (Tianjin University Children's Hospital), Tianjin, China.

Genet Med. 2023 Sep;25(9):100878. doi: 10.1016/j.gim.2023.100878. Epub 2023 Jun 5.

Abstract

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