UNUSUAL HETEROZYGOTES OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY CONFIRMED BY HLA TISSUE TYPING
- 1 November 1979
- journal article
- research article
- Published by Oxford University Press (OUP) in Acta Endocrinologica
- Vol. 92 (3) , 542-546
- https://doi.org/10.1530/acta.0.0920542
Abstract
In a previous publication, 3 relatives of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency from 2 families were considered to be unusual heterozygotes rather than homozygotes with mild clinical manifestations. Their heterozygosity could now be confirmed by HLA tissue typing.This publication has 3 references indexed in Scilit:
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
- UNUSUAL HETEROZYGOTES OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCYActa Endocrinologica, 1978
- CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)The Lancet, 1977