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Of these, 27 were amyloid PET-negative and 33 PET-positive

PMID: 32110280

They believe it was the result of deoxycholic acid being injected improperly

K404E or this mutation with a null allele leads to severe deficiency of CPOX, and to a disorder characterized by jaundice, anemia, hepato-splenomegaly often occurring in the neonatal period, with later photosensitivity, as seen in hepato-erythropoietic porphyria, porphyria cutanea tarda congenital erythropoietic porphyria, and variegate porphyria

TP53 mutations TP53 mutations occur in approximately 50% of NSCLC cases and are associated with aggressive tumor behavior and poor prognosis

This kind of regular repetition and high glycine content is found in only a few other fibrous proteins, such as silk fibroin (75-80% Gly and Ala + 10% Ser)
