Cite
HARVARD Citation
Wheeler, P. et al. (2016). SRD5A3‐CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features. American journal of medical genetics. 170 (12), pp. 3165-3171. [Online].
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Wheeler, P. et al. (2016). SRD5A3‐CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features. American journal of medical genetics. 170 (12), pp. 3165-3171. [Online].