Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency (Q37310420)
Jump to navigation
Jump to search
scientific article published on August 2009
Language | Label | Description | Also known as |
---|---|---|---|
English | Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency |
scientific article published on August 2009 |
Statements
1 reference
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency (English)
1 reference
Martin O Savage
1 reference
Adrian J L Clark
1 reference
Louise A Metherell
1 reference
Li F Chan
1 reference
Heiko Krude
1 reference
Colin Ball
1 reference
Stephen M P O'Riordan
1 reference
Colm Costigan
1 reference
Sally A Lynch
1 reference
Paolo Cavarzere
1 reference
1 reference
1 reference
Identifiers
1 reference