<Record><identifier xmlns="http://purl.org/dc/elements/1.1/">URN:NBN:SI:doc-14DFTUDW</identifier><date>2022</date><creator>Burgar, Jan</creator><creator>Fakin, Ana</creator><creator>Glavač, Damjan</creator><creator>Hawlina, Marko</creator><creator>Jarc-Vidmar, Martina</creator><creator>Petrović Pajić, Sanja</creator><creator>Šega, Rok</creator><creator>Volk, Marija</creator><relation>documents/doc/1/URN_NBN_SI_doc-14DFTUDW_001.pdf</relation><relation>documents/doc/1/URN_NBN_SI_doc-14DFTUDW_001.txt</relation><relation>documents/doc/1/URN_NBN_SI_doc-14DFTUDW_002.pdf</relation><relation>documents/doc/1/URN_NBN_SI_doc-14DFTUDW_002.txt</relation><format format_type="issue">9/10</format><format format_type="volume">91</format><format format_type="type">article</format><format format_type="extent">str. 398-411</format><identifier identifier_type="DOI">10.6016/ZdravVestn.3234</identifier><identifier identifier_type="ISSN">1318-0347</identifier><identifier identifier_type="COBISSID_HOST">178657283</identifier><identifier identifier_type="URN">URN:NBN:SI:doc-14DFTUDW</identifier><language>slv</language><publisher publisher_location="Ljubljana">Slovensko zdravniško društvo</publisher><source>Zdravniški vestnik</source><rights>BY-NC</rights><subject language_type_id="eng">amblyopia</subject><subject language_type_id="eng">genetics</subject><subject language_type_id="slv">genetika</subject><subject language_type_id="eng">mitochondrial diseases</subject><subject language_type_id="slv">mitohondrijske bolezni</subject><subject language_type_id="slv">slabovidnost</subject><title>Leberjeva hereditarna optična nevropatija</title><title>pregled bolezni z analizo prisotnosti v Sloveniji</title><title>Leber’s hereditary optic neuropathy</title><title>a review and prevalence analysis in the Slovenian population</title></Record>