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 journal › Letter

11 Citations (Scopus)
LanguageEnglish
Pages543-547
Number of pages5
JournalJournal of Medical Genetics
Volume37
Issue number7
DOIs
Publication statusPublished - 1 Jul 2000
Externally publishedYes

Cite this

Boyne, J. ; Evans, Steve ; Pollitt, Rodney J. ; Taylor, Christopher J. ; Dalton, Ann. / Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation. In: Journal of Medical Genetics. 2000 ; Vol. 37, No. 7. pp. 543-547.
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Boyne, J, Evans, S, Pollitt, RJ, Taylor, CJ & Dalton, A 2000, 'Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation', Journal of Medical Genetics, vol. 37, no. 7, pp. 543-547. https://doi.org/10.1136/jmg.37.7.543

Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation. / Boyne, J.; Evans, Steve; Pollitt, Rodney J.; Taylor, Christopher J.; Dalton, Ann.

In: Journal of Medical Genetics, Vol. 37, No. 7, 01.07.2000, p. 543-547.

Research output: Contribution to journal › Letter

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Boyne J, Evans S, Pollitt RJ, Taylor CJ, Dalton A. Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation. Journal of Medical Genetics. 2000 Jul 1;37(7):543-547. https://doi.org/10.1136/jmg.37.7.543

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