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Case report: A novel PPP3CA truncating mutation within the regulatory domain causes severe developmental and

Jieling Li1,2, Jie Cao1,2

  • 1Department of Medical General Ward, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing, China.

Frontiers in Neurology
|September 26, 2022
PubMed
Abstract

Keywords:
DEE91PPP3CAcase reportepilepsyregulatory domain

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