Montalbano et al., 2016 - Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. EMBO Molecular Medicine   8(12):1455-1469 Full text @ EMBO Mol. Med.
Human Disease / Model Data (1 Record)
Human Disease Fish Environment Evidence Code
Leri-Weill dyschondrosteosis
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