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EC Number Application Commentary Reference
Show all pathways known for 1.3.1.94Display the word mapDisplay the reaction diagram Show all sequences 1.3.1.94medicine loss of function mutations of the SRD5A3 gene cause a multisystemic syndrome with eye malformations, cerebellar vermis hypoplasia, and psychomotor delay. Plasma from patients shows increased level of polyprenoids 719256
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