Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency

Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency

Bibliographic Details
Main Authors: Chan, Li F, Metherell, Louise A, Krude, Heiko, Ball, Colin, O'Riordan, Stephen M P, Costigan, Colm, Lynch, Sally A, Savage, Martin O, Cavarzere, Paolo, Clark, Adrian J L
Format: Online
Language:English
Published: Blackwell Publishing Ltd 2009
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728896/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728896/

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