Publication | Closed Access
Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms
27
Citations
42
References
2012
Year
Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseHuman PolymorphismPathologyMolecular GeneticsNovel PolymorphismsTunisian PatientsMedicineClinical Genetics
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