The PvuII restriction site in the second intron of the human steroid 21-hydroxylase gene CYP21 is polymorphic

Clin Genet. 1995 Aug;48(2):109-10. doi: 10.1111/j.1399-0004.1995.tb04066.x.

Authors

P F Koppens¹, T Hoogenboezem, H J Degenhart

Affiliation

¹ Department of Paediatrics, University Hospital Rotterdam, Sophia Children's Hospital, The Netherlands.

PMID: 7586650
DOI: 10.1111/j.1399-0004.1995.tb04066.x

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Deoxyribonucleases, Type II Site-Specific / genetics*
Genetic Markers*
Humans
Introns
Polymorphism, Genetic*
Steroid 21-Hydroxylase / genetics*

Substances

Genetic Markers
Steroid 21-Hydroxylase
CAGCTG-specific type II deoxyribonucleases
Deoxyribonucleases, Type II Site-Specific