Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 (Q28302878)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 |
scientific article |
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Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 (English)
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February 2005
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37
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2
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166-70
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