Pseudohypoaldosteronism type II and sensory neuropathy associated with a heterozygous pathogenic variant in KLHL3 gene, a case report
假性醛固酮增多症II型和感觉神经病与KLHL3基因杂合致病变异相关的病例报告
期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2024.e39891
Davion, J B; Coku, I; Wissocq, A; Genet, A; Poupart, J; Defebvre, L; Huin, V
