Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2 - Concepedia

Concepedia

Publication | Closed Access

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

444

Citations

24

References

2005

Year

Louise Metherell, J. Paul Chapple, Sadani N. Cooray, Alessia David, Christian Becker, Franz Rüschendorf, Danielle Naville, Martine Bégeot, Bernard Khoo, Peter Nürnberg,

Nature Genetics

Mendelian DisorderAutoimmune DiseaseNew Interacting PartnerGenetic DisorderGeneticsPathologyDegenerative DiseaseInborn Error Of ImmunityActh ReceptorGlucocorticoidMedicineLysosomal Storage Disease

References

	Year	Citations

Page 1

Page 1