Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation

J. Boyne, Steve Evans, Rodney J. Pollitt, Christopher J. Taylor, Ann Dalton

Research output: Contribution to journalLetter

12 Citations (Scopus)
Original languageEnglish
Pages (from-to)543-547
Number of pages5
JournalJournal of Medical Genetics
Volume37
Issue number7
DOIs
Publication statusPublished - 1 Jul 2000
Externally publishedYes

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