The spectrum of clinical disease in hyperekplexia: genotype and phenotype of forty-two cases [Conference Abstract]

Thomas, Rhys Huw ORCID: https://orcid.org/0000-0003-2062-8623, Chung, S. K., Rees, M. I., Robinson, A. and Hammond, C. L. 2010. The spectrum of clinical disease in hyperekplexia: genotype and phenotype of forty-two cases [Conference Abstract]. Developmental Medicine & Child Neurology 52 , p. 13. 10.1111/j.1469-8749.2009.03574.x

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Item Type:	Article
Status:	Published
Schools:	Schools > Medicine Research Institutes & Centres > MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Subjects:	R Medicine > R Medicine (General) R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Publisher:	Wiley-Blackwell
ISSN:	0012-1622
Last Modified:	01 Nov 2022 09:41
URI:	https://orca.cardiff.ac.uk/id/eprint/88852

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