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Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia. [electronic resource] by
- Bolar, Nikhita Ajit
- Golzio, Christelle
- Živná, Martina
- Hayot, Gaëlle
- Van Hemelrijk, Christine
- Schepers, Dorien
- Vandeweyer, Geert
- Hoischen, Alexander
- Huyghe, Jeroen R
- Raes, Ann
- Matthys, Erve
- Sys, Emiel
- Azou, Myriam
- Gubler, Marie-Claire
- Praet, Marleen
- Van Camp, Guy
- McFadden, Kelsey
- Pediaditakis, Igor
- Přistoupilová, Anna
- Hodaňová, Kateřina
- Vyleťal, Petr
- Hartmannová, Hana
- Stránecký, Viktor
- Hůlková, Helena
- Barešová, Veronika
- Jedličková, Ivana
- Sovová, Jana
- Hnízda, Aleš
- Kidd, Kendrah
- Bleyer, Anthony J
- Spong, Richard S
- Vande Walle, Johan
- Mortier, Geert
- Brunner, Han
- Van Laer, Lut
- Kmoch, Stanislav
- Katsanis, Nicholas
- Loeys, Bart L
Producer: 20170519
In:
American journal of human genetics vol. 99
Availability: No items available.
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