M. Konrad Et Al. , "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.," American journal of human genetics , vol.79, no.5, pp.949-57, 2006
Konrad, M. Et Al. 2006. Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.. American journal of human genetics , vol.79, no.5 , 949-57.
Konrad, M., Schaller, A., Seelow, D., Pandey, A. V., Waldegger, S., Lesslauer, A., ... Vitzthum, H.(2006). Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.. American journal of human genetics , vol.79, no.5, 949-57.
Konrad, Martin Et Al. "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.," American journal of human genetics , vol.79, no.5, 949-57, 2006
Konrad, Martin Et Al. "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.." American journal of human genetics , vol.79, no.5, pp.949-57, 2006
Konrad, M. Et Al. (2006) . "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.." American journal of human genetics , vol.79, no.5, pp.949-57.
@article{article, author={Martin Konrad Et Al. }, title={Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.}, journal={American journal of human genetics}, year=2006, pages={949-57} }