Comprehensive analytical strategy for mutation screening in 21- hydroxylase deficiency

Clinical Chemistry

Volumn 44, Issue 10, 1998, Pages 2075-2082

  Krone, Nils ^a   Roscher, Adelbert Anton ^a   Schwarz, Hans Peter ^a   Braun, Andreas ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYPROGESTERONE; PREGNANETRIOL; RENIN; STEROID 21 MONOOXYGENASE;

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONGENITAL ADRENAL HYPERPLASIA; DIAGNOSTIC ACCURACY; DNA SEQUENCE; FEMALE; GENE ACTIVATION; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MASS SCREENING; PSEUDOGENE; SALT LOSING NEPHRITIS; SOUTHERN BLOTTING; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 0031712054     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/44.10.2075     Document Type: Article

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