Publications

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Filters: Keyword is 3-Oxo-5-alpha-Steroid 4-Dehydrogenase  [Clear All Filters]
2016
Wheeler, P. G. et al. SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features. Am J Med Genet A 170, 3165-3171 (2016).