Association of clinical severity of cystic fibrosis with variants in the SLC gene family ( SLC6A14 , SLC26A9 , SLC11A1 and SLC9A3 )
Author:
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference42 articles.
1. Human solute carrier SLC6A14 is the β-alanine carrier;Anderson;J. Physiol.,2008
2. Genetic variants of SLC11A1 are associated with both autoimmune and infectious diseases: systematic review and meta-analysis;Archer;Genes Immun.,2015
3. SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia;Bertrand;J. Gen. Physiol.,2009
4. Genetic modifiers of cystic fibrosis-related diabetes;Blackman;Diabetes,2013
5. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease;Bonadia;Gene,2014
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