Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.
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B. Boehm | A. Wissmann | S. Maier | H. Dralle | W. Karges | B. Feldmann | K. Jostarndt | M. Weitz | A. Flemming | P. Wagner | H. Dralle