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August 15, 2024

[Clinical and genetic features of children with 3-methylcrotonyl-coenzyme A carboxylase deficiency: an analysis of six cases].

Liming Zhang Shengnan Wu Y. Guo Jianwei Yang Hongqi Sun Junmei Yang Yongxing Chen

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Abstract

To investigate the clinical and genetic features of children with 3-methylcrotonyl-coenzyme A carboxylase deficiency (MCCD).

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Cite This Study

Zhang et al. (2024) studied this question.

synapsesocial.com/papers/68e5c1f9b6db643587559e02 https://doi.org/10.7499/j.issn.1008-8830.2404026

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Keep reading

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1An asymptomatic father diagnosed with 3-methylcrotonyl-CoA carboxylase deficiency following his son newborn screening test2024 · 2 citations
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