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Tanaka R, Ichimura Y, Kubota N, et al
The type II form represents about 5% of all cases of CGD and is the result of mutations in the NFC2 gene which encodes the p67-PHOX protein
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[12] mhra.gov.uk or through the Yellow Card app
S., & Rubenstein, J
How Retinol Works: Forced Cellular Turnover Retinol is a vitamin A derivative
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