Multiple transcripts of the CYP21 gene are generated by the mutation of the splicing donor site in nitron 2 from GT to AT in 21-hydroxylase deficiency

Journal of Endocrinology

Volumn 171, Issue 3, 2001, Pages 397-402

  Lee, H H ^a   Chang, S F ^a  

^a Kingcar Food Industrial Co Ltd   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; GUANINE; MESSENGER RNA; RNA; STEROID 21 MONOOXYGENASE; THYMINE;

ANIMAL CELL; ARTICLE; BINDING SITE; CELL STRAIN COS1; CONTROLLED STUDY; DONOR SITE; GENE CONSTRUCT; GENE DELETION; GENE MUTATION; GENETIC ANALYSIS; GENETIC TRANSFECTION; INTRON; MUTANT; NONHUMAN; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; RNA TRANSCRIPTION; STEROID 21 MONOOXYGENASE DEFICIENCY;

ADRENAL HYPERPLASIA, CONGENITAL; ANIMALS; BASE SEQUENCE; COS CELLS; GENE EXPRESSION; HUMANS; INTRONS; MOLECULAR SEQUENCE DATA; POINT MUTATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA SPLICING; STEROID 21-HYDROXYLASE; TRANSCRIPTION, GENETIC; TRANSFECTION;

EID: 0035664387     PISSN: 00220795     EISSN: None     Source Type: Journal    
DOI: 10.1677/joe.0.1710397     Document Type: Article

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12. Homologous sequences in steroidogenic enzymes, steroid receptors and a steroid binding protein suggest a consensus steroid-binding sequence
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16. Unusual splice sites revealed by mutagenic inactivation of an authentic splice site of the rabbit β-globin gene