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Paper Details

GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease.
PLoS One
32
2011
CNV, CNVs, DNA copy number variants, GALC, GALC deletions, Krabbe disease, Mendelian variants, POAG, Primary Open Angle Glaucoma, autism, galactosylceramidase, galactosylceramidase gene, human, inherited disorders, optic neuropathy, patients, primary open-angle glaucoma, recessive Mendelian disorder, schizophrenia, vision loss
Author NameAffiliation
Yutao LiuCenter for Human Genetics, Duke University Medical Center
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Datasets

dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink
dbGaPDatabase of Genotypes and PhenotypesLink