SLC52A2 mutations cause SCABD2 phenotype: A second report

International Journal of Pediatric Otorhinolaryngology 2018 / 01 Vol. 104

SLC52A2 mutations cause SCABD2 phenotype: A second report

Babanejad, Mojgan, Adeli, Omid Ali, Nikzat, Nooshin, Beheshtian, Maryam, Azarafra, Hakimeh, Sadeghnia, Farnaz, Mohseni, Marzieh, Najmabadi, Hossein, Kahrizi, Kimia
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Volume:
104
Language:
english
Journal:
International Journal of Pediatric Otorhinolaryngology
DOI:
10.1016/j.ijporl.2017.11.014
Date:
January, 2018
File:
PDF, 565 KB
english, 2018
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