Publication | Closed Access
Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Further evidence for different allelic variants at the 21-hydroxylase locus
50
Citations
28
References
1982
Year
Adrenal GlandGenetic DisorderMedicineGeneticsAdrenal HealthInherited Metabolic DiseasePathology21-Hydroxylase LocusAdrenal DiseaseComplement C421-Hydroxylase DeficiencyInborn Error Of ImmunityMolecular Medicine
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