Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice. [electronic resource]
Producer: 20050628Description: 2563-74 p. digitalISSN:- 0013-7227
- Adrenal Hyperplasia, Congenital -- genetics
- Amino Acid Sequence
- Animals
- Base Sequence
- Blotting, Southern
- Codon, Nonsense
- Crossing Over, Genetic
- Disease Models, Animal
- Gene Expression Regulation, Developmental
- Gene Expression Regulation, Enzymologic
- Genotype
- Mice
- Mice, Inbred C57BL
- Mice, Mutant Strains
- Microsatellite Repeats
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Mutation, Missense
- Polymerase Chain Reaction
- Protein Structure, Tertiary
- Pseudogenes -- genetics
- RNA, Messenger -- analysis
- Steroid 21-Hydroxylase -- chemistry
- Structure-Activity Relationship
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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