Rees, M. I., Baer, K., Ward, H., Coleman, Sharon Louise, Evans, I. L., Miller, J., Waldvogel, H., Faull, R. L. M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Snell, R. G. 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) , p. 627. |
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) Neuroscience and Mental Health Research Institute (NMHRI) |
Subjects: | R Medicine > R Medicine (General) |
Publisher: | Elsevier |
ISSN: | 0002-9297 |
Last Modified: | 25 Oct 2022 10:13 |
URI: | https://orca.cardiff.ac.uk/id/eprint/61444 |
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