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BPC-157 ()
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
Though no single isolate produced TMA, 2 subcommunities out of 768 did produce TMA, and 1 of those subcommunities was further fractionated using a similar strategy as before (i.e., single, 23, and 45 colonies
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