Browsing Centre for Endocrinology by Author "O'Riordan, SMP"
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Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
Chan, LF; Metherell, LA; Krude, H; Ball, C; O'Riordan, SMP; Costigan, C; Lynch, SA; Savage, MO; Cavarzere, P; Clark, AJL (2009-08)