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Zou et al., 2025)
The inclusion of Succinylacetone as marker for Tyrosinemia type I in expanded newborn screening programs
Primera prdida de pulgadas medible
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[7] Although SPCD is an autosomal recessive condition, heterozygotes have been shown to be at an increased risk for developing benign cardiomyopathy compared to wild type individuals
doi: 10.2337/diab.37.10.1358
