Results
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481.
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489.
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Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability. [electronic resource] by
- Schlingmann, Karl P
- Bandulik, Sascha
- Mammen, Cherry
- Tarailo-Graovac, Maja
- Holm, Rikke
- Baumann, Matthias
- König, Jens
- Lee, Jessica J Y
- Drögemöller, Britt
- Imminger, Katrin
- Beck, Bodo B
- Altmüller, Janine
- Thiele, Holger
- Waldegger, Siegfried
- Van't Hoff, William
- Kleta, Robert
- Warth, Richard
- van Karnebeek, Clara D M
- Vilsen, Bente
- Bockenhauer, Detlef
- Konrad, Martin
Producer: 20190514
In:
American journal of human genetics vol. 103
Availability: No items available.
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490.
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491.
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492.
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496.
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497.
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Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting. [electronic resource] by
- Will, Constanze
- Breiderhoff, Tilman
- Thumfart, Julia
- Stuiver, Marchel
- Kopplin, Kathrin
- Sommer, Kerstin
- Günzel, Dorothee
- Querfeld, Uwe
- Meij, Iwan C
- Shan, Qixian
- Bleich, Markus
- Willnow, Thomas E
- Müller, Dominik
Producer: 20120918
In:
American journal of physiology. Renal physiology vol. 298
Availability: No items available.
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498.
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Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia. [electronic resource] by
- Sugihara, Shinobu
- Hisatome, Ichiro
- Kuwabara, Masanari
- Niwa, Koichiro
- Maharani, Nani
- Kato, Masahiko
- Ogino, Kazuhide
- Hamada, Toshihiro
- Ninomiya, Haruaki
- Higashi, Yukihito
- Ichida, Kimiyoshi
- Yamamoto, Kazuhiro
Producer: 20160125
In:
Circulation journal : official journal of the Japanese Circulation Society vol. 79
Availability: No items available.
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499.
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500.
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