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UnknownNewly identified disorder of copper metabolism caused by variants in CTR1, a high-affinity copper transporter.
Not available
S-EPMC9759326 | biostudies-literature
UnknownMutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.
Not available
S-EPMC3257879 | biostudies-literature
UnknownResearch challenges in central nervous system manifestations of inborn errors of metabolism.
Not available
S-EPMC3040279 | biostudies-literature
UnknownPhase 2 Placebo-Controlled Trial of Two Vaccines to Prevent Ebola in Liberia.
Not available
S-EPMC5705229 | biostudies-literature
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