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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Publishing Ltd
2010
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| 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 |