NOVEL NONSENSE MUTATION (W302X) IN THE STEROID 21-HYDROXYLASE GENE OFA FINNISH PATIENT WITH THE SALT-WASTING FORM OF CONGENITAL ADRENAL-HYPERPLASIA

Authors
LEVO A PARTANEN J
Citation
A. Levo et J. Partanen, NOVEL NONSENSE MUTATION (W302X) IN THE STEROID 21-HYDROXYLASE GENE OFA FINNISH PATIENT WITH THE SALT-WASTING FORM OF CONGENITAL ADRENAL-HYPERPLASIA, Human mutation, 9(4), 1997, pp. 363-365
Citations number
9
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Volume
9
Issue
4
Year of publication
1997
Pages
363 - 365
Database
ISI
SICI code
1059-7794(1997)9:4<363:NNM(IT>2.0.ZU;2-P