Publication | Open Access
Structural Basis of a Point Mutation that Causes the Genetic Disease Aspartylglucosaminuria
12
Citations
30
References
2014
Year
Genetic Disease AspartylglucosaminuriaSomatic VariantMendelian DisorderGenetic DisorderGeneticsPathogenesisInherited Metabolic DiseaseMolecular BiologyPoint MutationStructural BasisMolecular GeneticsDisease Gene IdentificationMedicineClinical Genetics
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