SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the NF1 phenotype

Spurlock, G, Bennett, E, Chuzhanova, N ORCID: https://orcid.org/0000-0002-4655-3618, Thomas, N, Hoi-Ping, J, Side, L, Davies, S, Haan, E, Kerr, K, Huson, SM and Upadhyaya, M, 2009. SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the NF1 phenotype. Journal of Medical Genetics, 46, pp. 431-437.

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Item Type:	Journal article
Publication Title:	Journal of Medical Genetics
Creators:	Spurlock, G., Bennett, E., Chuzhanova, N., Thomas, N., Hoi-Ping, J., Side, L., Davies, S., Haan, E., Kerr, K., Huson, S.M. and Upadhyaya, M.
Date:	2009
Volume:	46
Divisions:	Schools > School of Science and Technology
Record created by:	EPrints Services
Date Added:	09 Oct 2015 10:20
Last Modified:	09 Jun 2017 13:26
URI:	https://irep.ntu.ac.uk/id/eprint/11439

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