Functional analysis of four CYP21 mutations from spanish patients with congenital adrenal hyperplasia. [electronic resource]
Producer: 19991007Description: 635-7 p. digitalISSN:- 0006-291X
- 17-alpha-Hydroxyprogesterone -- metabolism
- Adrenal Hyperplasia, Congenital -- enzymology
- Amino Acid Substitution
- Animals
- CHO Cells
- Cricetinae
- Gene Conversion
- Humans
- Mutagenesis, Site-Directed
- Mutation, Missense
- Point Mutation
- Progesterone -- metabolism
- Pseudogenes
- Recombinant Proteins -- metabolism
- Recombination, Genetic
- Spain
- Steroid 21-Hydroxylase -- genetics
- Substrate Specificity
- Transfection
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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