Items where Author is "Nikzat, Nooshin"

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Babanejad, Mojgan and Adeli, Omid Ali and Nikzat, Nooshin and Beheshtian, Maryam and Azarafra, Hakimeh and Sadeghnia, Farnaz and Mohseni, Marzieh and Najmabadi, Hossein and Kahrizi, Kimia (2018) SLC52A2 mutations cause SCABD2 phenotype: A second report. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 104. pp. 195-199. ISSN 0165-5876

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