APA

Weber S., Schneider L., Peters M., Misselwitz J., Rönnefarth G., Böswald M., Bonzel K. E., Seeman T., Suláková T., Kuwertz-Bröking E., Gregoric A., Palcoux J., Tasic V., Manz F., Schärer K., Seyberth H. W. & Konrad M. (20011204). Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. : Journal of the American Society of Nephrology : JASN.

Chicago

Weber Stefanie, Schneider Linda, Peters Melanie, Misselwitz Joachim, Rönnefarth Gabriele, Böswald Michael, Bonzel Klaus E, Seeman Tomas, Suláková Tereza, Kuwertz-Bröking Eberhard, Gregoric Alojz, Palcoux Jean-Bernard, Tasic Velibor, Manz Friedrich, Schärer Karl, Seyberth Hannsjörg W and Konrad Martin. 20011204. Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. : Journal of the American Society of Nephrology : JASN.

Harvard

Weber S., Schneider L., Peters M., Misselwitz J., Rönnefarth G., Böswald M., Bonzel K. E., Seeman T., Suláková T., Kuwertz-Bröking E., Gregoric A., Palcoux J., Tasic V., Manz F., Schärer K., Seyberth H. W. and Konrad M. (20011204). Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. : Journal of the American Society of Nephrology : JASN.

MLA

Weber Stefanie, Schneider Linda, Peters Melanie, Misselwitz Joachim, Rönnefarth Gabriele, Böswald Michael, Bonzel Klaus E, Seeman Tomas, Suláková Tereza, Kuwertz-Bröking Eberhard, Gregoric Alojz, Palcoux Jean-Bernard, Tasic Velibor, Manz Friedrich, Schärer Karl, Seyberth Hannsjörg W and Konrad Martin. Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. : Journal of the American Society of Nephrology : JASN. 20011204.