Work

Hyperekplexia in Kurdish families: A possible GLRA1 founder mutation

Year: 2006

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/01.wnl.0000223347.73493.af

Authors: A. Sirén, B. Legros, L. Chahine, J. -P. Misson, M. Pandolfo

Institutions: Erasmus Hospital, Tampere University Hospital, Centre hospitalier régional de la Citadelle

Language: English

Topic: Neuroscience and Neuropharmacology Research

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1989191515

FWCI: 0.127

Cites: 10

Cited by: 11

Related to: 10