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Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin

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3.2.1 Bifidobacterium breve As a key commensal representative, B

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GCN2 phosphorylates eIF2, leading to ATF4 induction and upregulation of downstream targets including CHAC1