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 journalArticlepeer-review

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

    Cite this