Publication | Closed Access
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome
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Citations
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References
2004
Year
Mendelian DisorderGenetic DisorderMedicineGeneticsPrincipal CauseMolecular GeneticsDisease Gene IdentificationGilbert SyndromeSystems BiologyPolymorphic MutationsMonogenic Disorders
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