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November 14, 2022Molecular Genetics and Metabolism ReportsOpen Access

Clinical and molecular investigation of 37 Japanese patients with multiple acyl-CoA dehydrogenase deficiency: p.Y507D in ETFDH, a common Japanese variant, causes a mortal phenotype

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Authors

KYKenji YamadaYOYoshimitsu OsawaHKHironori Kobayashi

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Yamada et al. (2022) studied this question.

synapsesocial.com/papers/6a0fc706d8c5cf602efd251chttps://doi.org/10.1016/j.ymgmr.2022.100940
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