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Browsing by Author Mayr, Johannes A
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2013 | Infantile peripheral neuropathy, deafness, and proximal tubulopathy associated with a novel mutation of the RRM2B gene: case study | Stojanovic, Vesna D   ; Mayr, Johannes A; Sperl, Wolfgang; Barisic, Nenad A ; Doronjski, Aleksandra R ; Milak, Gordana | Article | 21M21 |
| 2010 | NOVEL MITOCHONDRIAL DNA DELETION IN PATIENT WITH DISTINCT PRESENTATION OF PEARSON SYNDROME | Kecman, Bozica; Mayr, Johannes A; Djordjevic, Maja S; Sarajlija, Adrijan ; Stajic, Natasa | Conference Paper | Mp. category will be shown later |