Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucorticoid deficiency type 2
2004
Metherell, L.A. | Cooray, S. | Huebner, A. | Ruschendorf, F. | Naville, D. | Bégeot, Martine | Clark, A.J.
Bibliographic information
Other Subjects
Glucorticoide; Genetique; [info] computer science [cs]
Language
English
Type
Art
Source
Taylor & Francis
2021-03-15
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