Work

Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene

Year: 2010

Type: article

Study design: Case Report

Source: Journal of Neurology Neurosurgery & Psychiatry

DOI: 10.1136/jnnp.2009.177451

Authors: D. Hong, X. Luan, B. Chen, R. Zheng, W. Zhang, Z. Wang, Y. Yuan

Institution: Peking University First Hospital

Language: English

Topic: Ion channel regulation and function

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1986306621

FWCI: 0.65

Cites: 4

Cited by: 11

Related to: 10