The Turkish Journal of Pediatrics 2021 , Vol 63 , Num 4
Whole exome sequencing identifies a novel variant in ABCA3 in an individual with fatal congenital surfactant protein deficiency
Hayrunnisa Bekis Bozkurt 1 ,Yavuz Şahin 2
1 Department of Pediatrics, Kafkas University Faculty of Medicine, Kars
2 Genox Genetic Diseases Diagnostic Center, Ankara, Turkey
DOI : 10.24953/turkjped.2021.04.019 Keywords :
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