Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency
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C. Tsigos | A. Penhoat | D. Naville | G. Ocal | M. Berberoğlu | P. Durand | M. Bégeot | H. El Mourabit | H. E. Mourabit | A. Buronfosse | Gönül Öcal, | Philippe Durand | Armelle Penhoat