Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2021

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Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism Hydroxyacyl-CoA dehydrogenase deficiency leads to congenital hyperinsulinism. https://t.co/uib5E9xvTU https://t.co/oLFzunu7Gd

11 May 2022

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Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism #NeoPapers #neoTwitter https://t.co/qWUTHRLWYQ

15 Nov 2021

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Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism #NeoPapers #neoTwitter https://t.co/7Gh2BJK0fO

14 Nov 2021

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Genetic pathogenesis, diagnosis, and treatment of short-chain 3-hydroxyacyl-coenzyme A dehydrogenase hyperinsulinism #NeoPapers #neoTwitter https://t.co/wArsZoXFY8

13 Nov 2021

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