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Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Further evidence for different allelic variants at the 21-hydroxylase locus

Geoffrey J. O'Neill, Bo Dupont, Marilyn S. Pollack, Lenore S. Levine, Maria I. New

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Key concepts: Haplotype, C4A, Allele, Locus (genetics), Genetics, Biology, Null allele, Allele frequency

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Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Further evidence for different allelic variants at the 21-hydroxylase locus — Research Paper | ScholarLens