دورية أكاديمية
CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis
العنوان: | CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis |
---|---|
المؤلفون: | Konrad, Martin, Hou, Jianghui, Weber, Stefanie, Dötsch, Jörg, Kari, Jameela A, Seeman, Tomas, Kuwertz-Bröking, Eberhard, Peco-Antic, Amira, Tasic, Velibor, Dittrich, Katalin, Alshaya, Hammad O, von Vigier, Rodo O, Gallati, Sabina, Goodenough, Daniel A, Schaller, André |
المصدر: | Konrad, Martin; Hou, Jianghui; Weber, Stefanie; Dötsch, Jörg; Kari, Jameela A; Seeman, Tomas; Kuwertz-Bröking, Eberhard; Peco-Antic, Amira; Tasic, Velibor; Dittrich, Katalin; Alshaya, Hammad O; von Vigier, Rodo O; Gallati, Sabina; Goodenough, Daniel A; Schaller, André (2008). CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Journal of the American Society of Nephrology, 19(1), pp. 171-81. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1681/ASN.2007060709 |
بيانات النشر: | Lippincott Williams & Wilkins |
سنة النشر: | 2008 |
المجموعة: | BORIS (Bern Open Repository and Information System, University of Bern) |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
العلاقة: | https://boris.unibe.ch/23420Test/ |
الإتاحة: | https://doi.org/10.1681/ASN.2007060709Test https://boris.unibe.ch/23420Test/ |
حقوق: | info:eu-repo/semantics/restrictedAccess |
رقم الانضمام: | edsbas.151F3F6 |
قاعدة البيانات: | BASE |
الوصف غير متاح. |