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10.1002/ange.201903981 62 WangD.WuH.WangC.GuL.ChenH.JanaD.et al (2021)

Tyni T, Kivela T, Lappi M, Summanen P, Nikoskelainen E, Pihko H: Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy

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That said, I think knowing our genes is helpful, as it can provide us with a roadmap of knowing which areas may need more attention to minimize our symptoms

Better Yoo Podcast Listen to the BHRT Pellet Therapy episode and my interview about Hashimotos