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p.Phe508del , p.Gly542X , p.Arg1162X , p.Asn1303Lys , and p.Lys683serfsX38 mutations in CF newborn screening of Brazilian children

  • Published:2017-01-30 Issue:1 Volume:92 Page:115-116
  • ISSN:0009-9163
  • Container-title:Clinical Genetics
  • language:en
  • Short-container-title:Clin Genet

Author:

Ribas D.I.R.12,Escaliante C.H.2,Bortoli C.G.1,de Oliveira C.R.F.12,Mikami L.R.2,Riedi C.A.3,Raskin S.4,Rosário Filho N.A.13,Pereira-Ferrari L.12

Affiliation:

1. Postgraduate Program in Internal Medicine and Health Sciences; Hospital de Clínicas, Universidade Federal do Paraná; Curitiba Brazil

2. Centro Universitário Autônomo do Brasil -  Escola de Saúde, UniBrasil; Curitiba Brazil

3. Department of Pediatrics; Universidade Federal do Paraná, Hospital de Clínicas; Curitiba Brazil

4. Graduate Program in Health Sciences, School of Medicine School of Life Sciences; Pontifícia Universidade Católica do Paraná; Curitiba Brazil

Publisher

Wiley

Subject

Genetics(clinical),Genetics
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