Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain.

C. Mattocks, D. Baralle, P. Tarpey, C. ffrench-Constant, M. Bobrow, J. Whittaker

Research output: Contribution to journalArticlepeer-review

60 Citations (Scopus)
Original languageEnglish
Pages (from-to)e48
JournalJournal of Medical Genetics
Volume41
Issue number4
DOIs
Publication statusPublished - Apr 2004

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