Rees, M., Baer, K., Ward, H., Coleman, S., Evans, L., Miller, J., . . . Snell, R. (2001). A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. AMERICAN JOURNAL OF HUMAN GENETICS, 69(4), pp. 627-628.

Rees, Mark, et al. "A Missense Mutation of Human Gephyrin (GPHN) Is Associated With Hyperekplexia and Transcript Isoform Analysis Re-defines the Genomic Structure of GPHN." AMERICAN JOURNAL OF HUMAN GENETICS 69, no. 4 (2001): 627-628.

Rees, Mark, et al. "A Missense Mutation of Human Gephyrin (GPHN) Is Associated With Hyperekplexia and Transcript Isoform Analysis Re-defines the Genomic Structure of GPHN." AMERICAN JOURNAL OF HUMAN GENETICS 69.4 (2001): 627-628.