APA

Metherell L. A., Cooray S., Huebner A., Ruschendorf F., Naville D., Begeot M. & Clark A. J. L. (20050610). Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2. : Endocrine research.

Chicago

Metherell Louise A, Cooray Sadani, Huebner Angela, Ruschendorf Franz, Naville Danielle, Begeot Martine and Clark Adrian J L. 20050610. Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2. : Endocrine research.

Harvard

Metherell L. A., Cooray S., Huebner A., Ruschendorf F., Naville D., Begeot M. and Clark A. J. L. (20050610). Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2. : Endocrine research.

MLA

Metherell Louise A, Cooray Sadani, Huebner Angela, Ruschendorf Franz, Naville Danielle, Begeot Martine and Clark Adrian J L. Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2. : Endocrine research. 20050610.