Mutations in the genes encoding 11ß-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency.

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Bibliographic Details
Title: Mutations in the genes encoding 11ß-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency.
Authors: Draper, Nicole1, Walker, Elizabeth A.1, Bujalska, Iwona J.1, Tomlinson, Jeremy W.1, Chalder, Susan M.1, Arlt, Wiebke1, Lavery, Gareth G.1, Bedendo, Oliver1, Ray, David W.2, Laing, Ian3, Malunowicz, Ewa4, White, Perrin C.5, Hewison, Martin1, Mason, Philip J.6, Connell, John M.7, Shackleton, Cedric H.L.8, Stewart, Paul M.1
Source: Nature Genetics. Aug2003, Vol. 34 Issue 4, p434. 6p.
Database: Academic Search Ultimate
Description
ISSN:10614036
DOI:10.1038/ng1214