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PXDN

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

PXDN
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Peroxidasin homolog is a protein that in humans is encoded by the PXDN gene.[5][6][7]

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Peroxidasin requires ionic bromine as a co-factor, making bromine an essential element for human life.[8]

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Clinical significance

Mutations in PXDN are associated with microphthalmia.[9]

References

Further reading

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