Functional characterization of compound heterozygosity for GlyRα1 mutations in the startle disease hyperekplexia

• 作者Ruth Rea; Marina A. Tijssen; Colin Herd; Rune R. Frants; Dimitri M. Kullmann
• 卷第16卷
• 期第2期
• 印刷ISSN0953-816X
• 电子ISSN1460-9568
• 文件大小1276.25KB
• 发表时间2002
• DOI10.1046/j.1460-9568.2002.02054.x
• 页码186-196