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2015
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2005
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Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemia.
Not available
S-EPMC4509990
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biostudies-literature
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Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease.
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S-EPMC5471153
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biostudies-literature
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Biological validation of differentially expressed genes in chronic lymphocytic leukemia identified by applying multiple statistical methods to oligonucleotide microarrays.
Not available
S-EPMC1867538
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biostudies-literature
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