Point mutations abolish 11β-hydroxysteroid dehydrogenase type II activity in three families with the congenital syndrome of apparent mineralocorticoid excess

• 作者Paolo Ferrari; Varuni R. Obeyesekere; Kevin Li; Robert C. Wilson; Maria I. New; John W. Funder; Zygmunt S. Krozowski
• 卷第119卷
• 期第1期
• 印刷ISSN0303-7207
• 文件大小536.40KB
• 发表时间1996
• DOI10.1016/0303-7207(96)03787-2