Nasal Potential Difference in Cystic Fibrosis considering Severe CFTR Mutations

The gold standard for diagnosing cystic fibrosis (CF) is a sweat chloride value above 60 mEq/L. However, this historical and important tool has limitations; other techniques should be studied, including the nasal potential difference (NPD) test. CFTR gene sequencing can identify CFTR mutations, but...

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Detalles Bibliográficos
Autores principales: Ng, Ronny Tah Yen, Marson, Fernando Augusto de Lima, Ribeiro, Jose Dirceu, Ribeiro, Antonio Fernando, Bertuzzo, Carmen Silvia, Ribeiro, Maria Angela Gonçalves de Oliveira, Severino, Silvana Dalge, Sakano, Eulalia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312569/
https://www.ncbi.nlm.nih.gov/pubmed/25667564
http://dx.doi.org/10.1155/2015/306825

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312569/
https://www.ncbi.nlm.nih.gov/pubmed/25667564
http://dx.doi.org/10.1155/2015/306825

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