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HARVARD Citation
Hotz, A. et al. (2018). Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis. Human mutation. 39 (10), pp. 1305-1313. [Online].
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Hotz, A. et al. (2018). Mutation update for CYP4F22 variants associated with autosomal recessive congenital ichthyosis. Human mutation. 39 (10), pp. 1305-1313. [Online].