{{Rsnum
|rsid=111033737
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GALT
|position=34648379
|Gene_s=GALT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=111033737
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=34648376
|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.34648376C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
|Disease=Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000022164.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1518:C0268151:230400:352:79239:124354006
}}{{PMID Auto
|PMID=10408
|Title=Electrochemistry of drug action I: electrooreduction of ferredoxins.
}}

{{PMID Auto
|PMID=11216901
|Title=Galactosaemia and allelic variation at the galactose-1-phosphate uridyltransferase gene: a complex relationship between genotype and phenotype.
}}

{{PMID Auto
|PMID=12595586
|Title=Verbal dyspraxia and galactosemia.
}}

{{PMID Auto
|PMID=18210213
|Title=A yeast model reveals biochemical severity associated with each of three variant alleles of galactose-1P uridylyltransferase segregating in a single family.
}}

{{PMID Auto
|PMID=19224951
|Title=Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase.
|OA=1
}}

{{PMID Auto
|PMID=19375122
|Title=An update on the molecular analysis of classical galactosaemia patients diagnosed in Spain and Portugal: 7 new mutations in 17 new families.
}}