You are here

  • Home
  • Archive
  • Volume 42, Issue 7
  • Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer)

Article Text

Article menu
Download PDFPDF
Correspondence
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

Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

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

    View Full Text

    Footnotes

    • Competing interests: none declared