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Mutations in MRAP, encoding a new interacting partner of ... | ResearchHub
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Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
0
Authors
Lou Metherell
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Lou Metherell
•
J. Chapple
11 more
•
Adrian Clark
Published
January 16, 2005
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Journal
Nature Genetics
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Endocrine And Autonomic Systems
Show all topics
DOI
10.1038/ng1501
