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Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis

Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis

V. Scotet; M. De Braekeleer; M.-P. Audrézet; L. Lodé; C. Verlingue; I. Quéré; B. Mercier; I. Duguépéroux; J.-P. Codet; M.-P. Moineau; P. Parent; C. Férec
  • 作者V. Scotet; M. De Braekeleer; M.-P. Audrézet; L. Lodé; C. Verlingue; I. Quéré; B. Mercier; I. Duguépéroux; J.-P. Codet; M.-P. Moineau; P. Parent; C. Férec
  • 卷第59卷
  • 期第1期
  • 印刷ISSN0009-9163
  • 电子ISSN1399-0004
  • 文件大小72.16KB
  • 发表时间2001
  • DOI10.1034/j.1399-0004.2001.590107.x
  • 页码42-47
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