Heterozygous POR gene mutations in a patient with congenital adrenal hyperplasia
Endocrine
.
2022 Aug;77(2):401-402.
doi: 10.1007/s12020-022-03086-9.
Epub 2022 May 30.
Authors
Carmelo Gusmano
1
,
Aldo E Calogero
2
,
Rossella Cannarella
1
Affiliations
1
Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
2
Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy. aldo.calogero@unict.it.
PMID:
35635658
DOI:
10.1007/s12020-022-03086-9
No abstract available
MeSH terms
Adrenal Hyperplasia, Congenital* / genetics
Heterozygote
Humans
Mutation
Steroid 21-Hydroxylase / genetics
Substances
Steroid 21-Hydroxylase