SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

G Spurlock, E Bennett, N Chuzhanova, N Thomas, Jim H-Ping, L Side, S Davies, Eric Haan, B Kerr, S Huson, M Upadhyaya

    Research output: Contribution to journalArticle

    63 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)431-437
    Number of pages7
    JournalJournal of Medical Genetics
    Volume46
    Publication statusPublished - 2009

    Cite this

    Spurlock, G., Bennett, E., Chuzhanova, N., Thomas, N., H-Ping, J., Side, L., Davies, S., Haan, E., Kerr, B., Huson, S., & Upadhyaya, M. (2009). SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype. Journal of Medical Genetics, 46, 431-437.