Dias, RP; Chan, LF; Metherell, LA; Pearce, SH; Clark, AJ (2010) Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency. EUROPEAN JOURNAL OF ENDOCRINOLOGY, 162 (2). 357 - 359 (3). ISSN 0804-4643 https://doi.org/10.1530/EJE-09-0720
SGUL Authors: Clark, Adrian John L

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Item Type:	Article
Additional Information:	PubMed ID: 19903795
Keywords:	Addison Disease, Adolescent, Adult, Aged, Child, Female, Genotype, Glucocorticoids, Humans, Male, Membrane Proteins, Middle Aged, Mutation, Phosphoproteins, Polymorphism, Genetic, Promoter Regions, Genetic, Receptor, Melanocortin, Type 2, Young Adult, Science & Technology, Life Sciences & Biomedicine, Endocrinology & Metabolism, ACTH RECEPTOR, ADRENOCORTICOTROPIN RECEPTOR, ASSOCIATION, CHILDREN, Addison Disease, Adolescent, Adult, Aged, Child, Female, Genotype, Glucocorticoids, Humans, Male, Membrane Proteins, Middle Aged, Mutation, Phosphoproteins, Polymorphism, Genetic, Promoter Regions, Genetic, Receptor, Melanocortin, Type 2, Young Adult
Journal or Publication Title:	EUROPEAN JOURNAL OF ENDOCRINOLOGY
ISSN:	0804-4643
Related URLs:	Author
Dates:	Date Event 1 February 2010 Published
Web of Science ID:	WOS:000276611900020
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URI:	https://openaccess.sgul.ac.uk/id/eprint/100902
Publisher's version:	https://doi.org/10.1530/EJE-09-0720

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