Gangliosides

solute carrier family 33 member 1 ; Homo sapiens







2 Article(s)
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Title
Pub. Year
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1 22243965 Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin. 2012 Jan 13 2
2 10570973 Cloning and characterization of a putative mouse acetyl-CoA transporter cDNA. 1999 Oct 1 1