Chinese patients with p.Arg756 mutations of ATP1A3 : Clinical manifestations, treatment, and follow-up.
Weihua ZhangJiuwei LiXiuwei ZhuoJi ZhouWeixing FengShuai GongXiaotun RenChanghong DingTongli HanFang FangPublished in: Pediatric investigation (2022)
. However, the weakness and ataxia were variable. Phenotypic crossover and overlap were observed among these patients.