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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
  1. Correspondence to:
 Dr J Whittaker
 Regional Genetics Laboratories, Molecular Genetics, Kefford House, Maris Lane, Trumpington, Cambridge, CB2 2FF; joanne.whittakeraddenbrookes.nhs.uk
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Citation

Mattocks C, Baralle D, Tarpey P, et al
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

Publication history

  • Received June 30, 2003
  • Accepted November 21, 2003
  • Revised November 20, 2003
  • First published April 1, 2004.
Online issue publication 
April 01, 2004

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