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Deep resequencing of CFTR in 762 F508del homozygotes reveals clusters of non-coding variants associated with cystic fibrosis disease traits
Extensive phenotypic variability is commonly observed in individuals with Mendelian disorders, even among those with identical genotypes in the disease-causing gene. To determine whether variants within and surrounding CFTR contribute to phenotypic variability in cystic fibrosis (CF), we performed d...
Autores principales: | Vecchio-Pagán, Briana, Blackman, Scott M, Lee, Melissa, Atalar, Melis, Pellicore, Matthew J, Pace, Rhonda G, Franca, Arianna L, Raraigh, Karen S, Sharma, Neeraj, Knowles, Michael R, Cutting, Garry R |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121184/ https://www.ncbi.nlm.nih.gov/pubmed/27917292 http://dx.doi.org/10.1038/hgv.2016.38 |
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