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Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)
  1. J L Whittaker,
  2. C Mattocks,
  3. D Baralle,
  4. P Tarpey,
  5. C ffrench-Constant,
  6. M Bobrow
  1. Department of Medical Genetics, Box 134, Addenbrooke’s Hospital, Cambridge, UK
  1. Correspondence to:
 J L Whittaker
 Department of Medical Genetics, Box 134, Addenbrooke’s Hospital, Cambridge, UK; joanne.whittakeraddenbrookes.nhs.uk

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We are grateful to the authors for pointing out the errors in assignment of the predicted effect of some of the sequence variants that …

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  • Competing interests: none declared