المؤلفون: Müller, D, Hoenderop, J G, van Os, C H, J M Bindels, R

المصدر: Nephrology Dialysis Transplantation; July 2001, Vol. 16 Issue: 7 p1329-1335, 7p

المؤلفون: Müller D; Department of Cell Physiology, University Medical Centre Nijmegen, The Netherlands., Hoenderop JG, Vennekens R, Eggert P, Harangi F, Méhes K, Garcia-Nieto V, Claverie-Martin F, Os CH, Nilius B, J M Bindels R

المصدر: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 2002 Sep; Vol. 17 (9), pp. 1614-20.

نوع المنشور: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 8706402 Publication Model: Print Cited Medium: Print ISSN: 0931-0509 (Print) Linking ISSN: 09310509 NLM ISO Abbreviation: Nephrol Dial Transplant Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, Calcium/*urine , Calcium Channels/*genetics , Calcium Metabolism Disorders/*genetics, Adolescent ; Adult ; Aged ; Calcium Metabolism Disorders/urine ; Child ; Child, Preschool ; Chromosome Mapping ; Codon ; Europe ; Female ; Genes, Dominant ; Humans ; Male ; Middle Aged ; Open Reading Frames ; Pedigree ; Phenotype ; TRPV Cation Channels