Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency. [electronic resource]
Producer: 20040309Description: 214-20 p. digitalISSN:- 1096-7192
- Adrenal Hyperplasia, Congenital -- enzymology
- Alleles
- Base Sequence
- Complement C4b -- genetics
- Crossing Over, Genetic
- DNA Mutational Analysis
- Humans
- Mutation -- genetics
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Recombinant Fusion Proteins -- genetics
- Sequence Deletion
- Steroid 21-Hydroxylase -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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