DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Montalbano A, Juergensen L, Roeth R. , et al.
Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency.
EMBO Mol Med 2016;
8 (12) 1455-1469
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