دورية أكاديمية
أعرض في EDS

A Novel Mutation in Deficiency of 11 β-Hydroxylase: A Possible Association with Disease Severity.

التفاصيل البيبلوغرافية
العنوان: A Novel Mutation in Deficiency of 11 β-Hydroxylase: A Possible Association with Disease Severity.
المؤلفون: Kutbay, Nilüfer Özdemir1, Yürekli, Banu Şarer1, Şimşir, Ilgın Yıldırım1, Baykan, Emine Kartal1, Kocabaş, Gökçen Ünal1, Onay, Hüseyin2, Erdoğan, Mehmet1, Çetinkalp, Şevki1, Özgen, A.Gökhan1, Saygılı, L. Füsun1
المصدر: Journal of Clinical Research in Pediatric Endocrinology. 2015 Supplement, Vol. 7, p50-50. 1p.
مصطلحات موضوعية: *ADRENOGENITAL syndrome, *HYDROXYLASES
مستخلص: An abstract of the article "A Novel Mutation in Deficiency of 11 ß-Hydroxylase: A Possible Association with Disease Severity," by Nilüfer Özdemir Kutbay and colleagues is presented.
قاعدة البيانات: Academic Search Index
الوصف
تدمد:13085727