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Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTRmutation
  1. Dr Dalton,molecular.gen{at}sheffield.ac.uk
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Citation

BOYNE J, EVANS S, POLLITT RJ, et al
Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTRmutation

Publication history

  • First published July 1, 2000.
Online issue publication 
April 27, 2016

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