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

Cite this

@article{7b34f78078664652ae11a8880557986b,

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

author = "J. Boyne and Steve Evans and Pollitt, {Rodney J.} and Taylor, {Christopher J.} and Ann Dalton",

year = "2000",

month = jul,

day = "1",

doi = "10.1136/jmg.37.7.543",

language = "English",

volume = "37",

pages = "543--547",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "7",

}

TY - JOUR

T1 - Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation

AU - Boyne, J.

AU - Evans, Steve

AU - Pollitt, Rodney J.

AU - Taylor, Christopher J.

AU - Dalton, Ann

PY - 2000/7/1

Y1 - 2000/7/1

UR - http://www.scopus.com/inward/record.url?scp=0033624507&partnerID=8YFLogxK

U2 - 10.1136/jmg.37.7.543

DO - 10.1136/jmg.37.7.543

M3 - Letter

C2 - 10970190

AN - SCOPUS:0033624507

VL - 37

SP - 543

EP - 547

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

SN - 0022-2593

IS - 7

ER -