Back to search

Mutations of the ACTH receptor gene are only one cause of familial glucocorticoid deficiency

A. Weber, Adrian Clark
DOI: 10.1093/hmg/3.4.585
Human Molecular Genetics

Data up to Jan 2025

Published1994
Citations82
References0
Fields
BiologyMedicineEndocrinologyGeneticsInternal medicine

Total Citations Per Year

Abstract

References (0)

No references found

Cited By (0)

No citing papers found in database

Mutations of the ACTH receptor gene are only one cause of familial glucocorticoid… (1994) – Human Molecular Genetics | Metascience Observatory Explorer