Classical and nonclassical 21-hydroxylase deficiency: A molecular study of Argentine patients

Clinical Endocrinology

Volumn 56, Issue 2, 2002, Pages 239-245

  Dain, Liliana B ^a,b,c,d   Buzzalino, Noemí D ^a   Oneto, Adriana ^b   Belli, Susana ^b   Stivel, Mirta ^b   Pasqualini, Titania ^b   Minutolo, Carolina ^a,b   Charreau, Eduardo H ^b,c   Alba, Liliana G ^a  

^a Centro Nacional de Genética Médica   (Argentina)

^b UNIVERSIDAD DE BUENOS AIRES   (Argentina)

^c INST DE BIOL Y MED EXPERIMENTAL   (Argentina)

^d Centro Nacional de Genetica Medica de Buenos Aires   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; HYDROXYPROGESTERONE; STEROID 21 MONOOXYGENASE; STEROID HORMONE;

ADRENAL GLAND; ALLELE; ARGENTINA; ARTICLE; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; ENZYME DEFICIENCY; FEMALE; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOTE; HORMONE DETERMINATION; HUMAN; INTRON; MALE; MUTATION RATE; PARENT; POINT MUTATION; PREVALENCE; PRIORITY JOURNAL; SALT LOSING NEPHRITIS; SIBLING; VIRILIZATION;

17-ALPHA-HYDROXYPROGESTERONE; ADRENAL HYPERPLASIA, CONGENITAL; ADRENOCORTICOTROPIC HORMONE; ALLELES; ARGENTINA; FEMALE; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; POINT MUTATION; STEROID 21-HYDROXYLASE;

EID: 0036126404     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.0300-0664.2001.01419.x     Document Type: Article

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