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Genotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] allele
Cystic fibrosis (CF) is caused by CFTR (cystic fibrosis transmembrane conductance regulator) gene mutations. We ascertained five patients with a novel complex CFTR allele, with two mutations, H939R and H949L, inherited in cis in the same exon of CFTR gene, and one different mutation per patient inhe...
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| Hoofdauteurs: | , , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Sociedade Brasileira de Genética
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3168180/ https://ncbi.nlm.nih.gov/pubmed/21931512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S1415-47572011000300008 |
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