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HARVARD Citation
Lehmann, J. et al. (n.d.). An unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP/CS complex phenotype. British journal of dermatology. pp. 903-905. [Online].
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Lehmann, J. et al. (n.d.). An unusual mutation in the XPG gene leads to an internal in‐frame deletion and a XP/CS complex phenotype. British journal of dermatology. pp. 903-905. [Online].