<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:doc-TNIJOZ1Q</identifier><date>2020</date><creator>Kotnik Pirš, Ana</creator><creator>Krivec, Uroš</creator><creator>Trebušak Podkrajšek, Katarina</creator><relation>documents/doc/T/URN_NBN_SI_doc-TNIJOZ1Q_001.pdf</relation><relation>documents/doc/T/URN_NBN_SI_doc-TNIJOZ1Q_001.txt</relation><format format_type="issue">2</format><format format_type="volume">67</format><format format_type="type">article</format><format format_type="extent">str. 666-673</format><identifier identifier_type="DOI">10.17344/acsi.2019.5677</identifier><identifier identifier_type="ISSN">1580-3155</identifier><identifier identifier_type="COBISSID">20261123</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-TNIJOZ1Q</identifier><language>eng</language><publisher>Slovenian Chemical Society</publisher><publisher>Slovensko kemijsko društvo</publisher><source>Acta chimica slovenica</source><rights>BY</rights><subject language_type_id="slv">CFTR gen</subject><subject language_type_id="slv">cistična fibroza</subject><subject language_type_id="slv">registri bolnikov</subject><title>The c.3140-26A&gt;G variant of the CFTR gene in homozygous state causes mild cystic fibrosis - overview of longitudinal clinical data of the patient managed in our CF Center and review of the literature</title></Record>