The majority of adrenocorticotropin receptor (melanocortin 2 receptor) mutations found in familial glucocorticoid deficiency type 1 lead to defective trafficking of the receptor to the cell surface.
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| Description | scientific article published on 7 October 2008 |
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author: Lou Metherell Adrian J. L. Clark Paul Chapple Li F Chan |
| Publication date | October 7, 2008 |
| Language | English |
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