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Q38866800-2E56A2B1-DA49-430C-B69F-8BCFB59A2EDA
Q38866800-2E56A2B1-DA49-430C-B69F-8BCFB59A2EDA
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Statement
http://www.wikidata.org/entity/statement/Q38866800-2E56A2B1-DA49-430C-B69F-8BCFB59A2EDA
Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.
P2860
Q38866800-2E56A2B1-DA49-430C-B69F-8BCFB59A2EDA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38866800-2E56A2B1-DA49-430C-B69F-8BCFB59A2EDA
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wasDerivedFrom
4551550cd2afece57094b1f9807dca6a3a1c8bce
P2860
Biochemical and computational analyses of two phenotypically related GALT mutations (S222N and S135L) that lead to atypical galactosemia.