Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients

Primary periodic paralysis (PPP) is an inherited disorders of ion channel dysfunction characterized by recurrent episodes of flaccid muscle weakness, which can classified as hypokalemic (HypoPP), normokalemic ...

Source: Orphanet Journal of Rare Diseases - April 12, 2024 Category: Internal Medicine Authors: Xuechao Zhao, Haofeng Ning, Lina Liu, Chaofeng Zhu, Yinghui Zhang, Guifang Sun, Huanan Ren and Xiangdong Kong Tags: Research Source Type: research