Effects of individual mutations in the P-450(C21) pseudogene on the p-450(c21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiency

Journal of Biochemistry

Volumn 109, Issue 4, 1991, Pages 638-644

  Higashi, Yujiro ^a   Hiromasa, Takako ^a   Tanae, Ayako ^b   Miki, Tetsuo ^c   Nakura, Jun ^c   Kondo, Takuma ^d   Ohura, Toshihiro ^e   Ogawa, Eishin ^e   Nakayama, Kazuo ^f   Fujii kuriyama, Yoshiaki ^f  

^a CANCER INSTITUTE   (Japan)

^b NATIONAL CHILDREN S HOSPITAL   (Japan)

^c OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^d Children's Medical Center of Osaka City ^*  (Japan)

^e TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^f TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450;

ANIMAL CELL; ARTICLE; CASE REPORT; CHILD; GENE CONVERSION; HUMAN; MUTATION; NONHUMAN; PRIORITY JOURNAL; PSEUDOGENE; STEROID 21 MONOOXYGENASE DEFICIENCY;

ADRENAL HYPERPLASIA, CONGENITAL; BASE SEQUENCE; FEMALE; GENES, STRUCTURAL; HUMAN; KINETICS; MALE; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; MUTATION; OLIGONUCLEOTIDE PROBES; PSEUDOGENES; RECOMBINANT PROTEINS; RESTRICTION MAPPING; STEROID 21-HYDROXYLASE; SUPPORT, NON-U.S. GOV'T;

ANIMALIA;

EID: 0025753960     PISSN: 0021924X     EISSN: None     Source Type: Journal    
DOI: 10.1093/oxfordjournals.jbchem.a123433     Document Type: Article

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