A de novo inframe deletion variant in CAPZA2 tentacle domain with global developmental delay and secondary
Shanyu Pi1, Xiao Mao2, Hongyu Long1
1Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.
Clinical Genetics
|July 20, 2022
Abstract:
(A) Sanger sequencing confirmation and family pedigree for the patient. (B) A schematic representation of transcript and translation showing the positions of all CAPZA2 variants identified.


