{{Rsnum
|rsid=111033814
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=GALT
|position=34649535
|Gene_s=GALT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033814
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=34649532
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|GENEINFO=GALT:2592
|GENE_NAME=GALT
|GENE_ID=2592
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.34649532C>A
|CLNSRC=Emory University
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase; not provided
|Disease=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase; not provided
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000022266.1; RCV000078213.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1518:C0268151:230400:352:79239:124354006
|CLNSRCID=736
}}{{PMID|10408}} Electrochemistry of drug action I: electrooreduction of ferredoxins.

{{PMID|10535394}} Urine and plasma galactitol in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia.

{{PMID|10960497}} Galactose breath testing distinguishes variant and severe galactose-1-phosphate uridyltransferase genotypes.

{{PMID|11261429}} The molecular biology of galactosemia.

{{PMID|11754113}} Molecular analysis in newborns from Texas affected with galactosemia.

{{PMID|15172000}} Extended [13C]galactose oxidation studies in patients with galactosemia.