Publication | Closed Access
Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency
25
Citations
21
References
2000
Year
3-Hydroxy-3-methylglutaryl Coa LyaseGenetic DisorderGeneticsInherited Metabolic DiseasePathologyClinical AnalysisMedicineJapanese PatientsMolecular Medicine
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