Literature DB >> 3306838

Genetics of steroid 21-hydroxylase deficiency.

P C White.   

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Year:  1987        PMID： 3306838     DOI： 10.1016/b978-0-12-571143-2.50014-9

Source DB:  PubMed          Journal:  Recent Prog Horm Res        ISSN： 0079-9963


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  3 in total

Review 1.  21-Hydroxylase deficiency: from molecular genetics to clinical presentation.

Authors:  E Trakakis; D Laggas; E Salamalekis; G Creatsas
Journal:  J Endocrinol Invest       Date:  2005-02       Impact factor: 4.256

2.  Substitution of Ile-172 to Asn in the steroid 21-hydroxylase B (P450c21B) gene in a Finnish patient with the simple virilizing form of congenital adrenal hyperplasia.

Authors:  J Partanen; R D Campbell
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

3.  Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8.

Authors:  K M Curnow; L Slutsker; J Vitek; T Cole; P W Speiser; M I New; P C White; L Pascoe
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-15       Impact factor: 11.205
  3 in total

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