Work

Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy

Year: 2000

Type: article

Study design: Observational Study

Source: American Journal of Medical Genetics

DOI: 10.1002/(sici)1096-8628(20000207)96:1<8::aid-ajmg3>3.0.co;2-s

Authors: Kerstin Hallmann, Martina Durner, Thomas Sander, Ortrud K. Steinlein

Institutions: University of Bonn, Icahn School of Medicine at Mount Sinai, Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin

Language: English

Topic: Epilepsy research and treatment

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1975300331

FWCI: 0.932

Cites: 41

Cited by: 14

Related to: 10