Novel variation at chr11p13 associated with cystic fibrosis lung disease severity.

Hum Genome Var · 2016 · PMC4935763 · PMID 27408752

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highly significantno p-value reported

Highly significant associations were in strong linkage disequilibrium and were seen only in Phe508del homozygous CF subjects, indicating a CFTR genotype-specific mechanism. status released display-pdf yes is-olf no is-manuscript no is-preprint no is-journal-matter no is-scanned no is-retracted no Received 2016 Mar 14; Revised 2016 May 6; Accepted 2016 May 9; Collection date 2016.

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