Phenotypic characteristics of familial glucocorticoid deficiency (FGD) type 1 and 2

CONTEXT: Familial glucocorticoid deficiency (FGD) is a rare autosomal recessive disorder as a result of mutation in genes encoding either the ACTH receptor [melanocortin 2 receptor (MC2R)] or its accessory protein [melanocortin 2 receptor accessory protein (MRAP)[. The disorder is known as FGD type...

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Detalles Bibliográficos
Autores principales: Chung, Teng-Teng L L, Chan, Li F, Metherell, Louise A, Clark, Adrian J L
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855830/
https://www.ncbi.nlm.nih.gov/pubmed/19558534
http://dx.doi.org/10.1111/j.1365-2265.2009.03663.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855830/
https://www.ncbi.nlm.nih.gov/pubmed/19558534
http://dx.doi.org/10.1111/j.1365-2265.2009.03663.x

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