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<http://identifiers.org/pubmed/15654338> <http://purl.org/dc/terms/title> "Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2" <http://purl.org/np/RAETXgt89C89LIbHgjsxgLfL48vysAaSlG6WtsJRnATY8#provenance> .
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