Publication not explained

This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.

If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.

Featured Image

Read the Original

This page is a summary of: Missense Mutations in the Melanocortin 2 Receptor Accessory Protein That Lead to Late Onset Familial Glucocorticoid Deficiency Type 2, The Journal of Clinical Endocrinology & Metabolism, July 2010, Endocrine Society,
DOI: 10.1210/jc.2009-2731.
You can read the full text:

Read

Contributors

The following have contributed to this page