In a population of very low birth weight infants, sequencing of a variety of antioxidant genes revealed single-nucleotide polymorphisms in the NQO1 gene (coding for NADPH quinone reductase) and the NFE2L2 gene (coding for NRF2), which were associated significant differences in the risk of BPD [129]. The gene discussed is CRYZ; the disease is bronchopulmonary dysplasia.