Publications by authors named "Lauma Veidemane"

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The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
Viktorija Igumnova, Lauma Veidemane, Anda Vīksna, Valentina Capligina, Egija Zole

J Hum Genet· March 2019

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