Mutations in the Human Proopiomelanocortin Gene
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.2003.tb03185.x/fullpdf
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4. Isolated congenital ACTH deficiency: a cleavage enzyme defect? Clin;Nussey;Endocrinol. (Oxford),1993
5. A pituitary cell-restricted T box factor, Tpit, activates POMC transcription in cooperation with Pitx homeoproteins;Lamolet;Cell,2001
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