Monika Oldak
0000-0002-4216-9141
3 papers found
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Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in USH2A
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss
Application of next‑generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss
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