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Cystic fibrosis in Afro-Brazilians: XK haplotypes analysis supports the European origin of p.F508del mutation.
de Souza, D A S; Faucz, F R; de Alexandre, R B; Santana, M A; de Souza, E L S; Reis, F J C; Pereira-Ferrari, L; Sotomaior, V S; Culpi, L; Phillips, J A; Raskin, S.
Affiliation
  • de Souza DA; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil. denise_andreass@yahoo.com.br.
  • Faucz FR; Functional Genomics Laboratory, Carlos Chagas Institute, Oswaldo Cruz Foundation, Curitiba, Paraná, Brazil. denise_andreass@yahoo.com.br.
  • de Alexandre RB; , 61H Travessa Chile, São José dos Pinhais, Paraná, 83035-200, Brazil. denise_andreass@yahoo.com.br.
  • Santana MA; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil.
  • de Souza EL; Section on Endocrinology and Genetics, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, Bethesda, MD, 20892, USA.
  • Reis FJ; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil.
  • Pereira-Ferrari L; Octávio Mangabeira Hospital, Reference Center of Cystic Fibrosis, Salvador, Bahia, Brazil.
  • Sotomaior VS; Pediatric Division, Federal University of Bahia, Salvador, Bahia, Brazil.
  • Culpi L; Pneumology Division, Department of Pediatrics, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
  • Phillips JA; Department of Biomedicine, UniBrasil, Curitiba, Paraná, Brazil.
  • Raskin S; Group for Advanced Molecular Investigation (NIMA), School of Health and Biosciences, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba, Paraná, Brazil.
Genetica ; 145(1): 19-25, 2017 Feb.
Article in En | MEDLINE | ID: mdl-28160168
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Full text: 1 Database: MEDLINE Main subject: Haplotypes / Ethnicity / Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis / Mutation Type of study: Observational_studies / Risk_factors_studies Limits: Humans / Male Country/Region as subject: America do sul / Brasil Language: En Year: 2017 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Haplotypes / Ethnicity / Cystic Fibrosis Transmembrane Conductance Regulator / Cystic Fibrosis / Mutation Type of study: Observational_studies / Risk_factors_studies Limits: Humans / Male Country/Region as subject: America do sul / Brasil Language: En Year: 2017 Type: Article