Waisman Center
Advancing knowledge of human development, developmental disabilities, and neurodegenerative diseases.

Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin

Durkin, PhD, DrPH, M. S., and M. Baker, MD. Prevalence and Mutation Analysis of short/Branched Chain Acyl-CoA Dehydrogenase Deficiency (SBCADD) Detected on Newborn Screening in Wisconsin.

Van Calcar SC, Baker MW, Williams P, Jones SA, Xiong B, Thao MC, Lee S, Yang MK, Rice GM, Rhead W, Vockley J, Hoffman G, Durkin MS. (2013) Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin. Molecular Genetics and Metabolism. S1096-7192(13)00136-4.