Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor-Reference-Cited by-同舟云学术

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Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor

Published:1993-02 Issue:8843 Volume:341 Page:461-462
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Clark A.J.L.,Grossman A.,McLoughlin L.

Publisher

Elsevier BV

Subject

General Medicine

Reference9 articles.

1. Familial Addison's disease;Shepard;Am J Dis Child,1959

2. The syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six cases;Migeon;Pediatr Res,1968

3. Familial glucocorticoid deficiency: studies of diagnosis and pathogenesis;Thistlethwaite;Arch Dis Child,1975

4. Familial glucocorticoid deficiency with achaslasia of the cardia and deficient tear production;Allgrove;Lancet,1978

5. Hereditary adrenocortical unresponsiveness to adrenocorticotropin with postreceptor defect;Yamaoka;J Clin Endocrinol Metab,1992

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