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

✍ Scribed by Paolo Ferrari; Varuni R. Obeyesekere; Kevin Li; Robert C. Wilson; Maria I. New; John W. Funder; Zygmunt S. Krozowski

• Book ID: 116122789
• Publisher: Elsevier Science
• Year: 1996
• Tongue: English
• Weight: 536 KB
• Volume: 119
• Category: Article
• ISSN: 0303-7207
• DOI: 10.1016/0303-7207(96)03787-2