Kobson - Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association(Article)

Naslov	Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association (Article)
Autori	Saisawat Pawaree Kohl Stefan Hilger Alina C Hwang Daw-Yang Gee Heon Yung Dworschak Gabriel C Tasic Velibor Pennimpede Tracie Natarajan Sivakumar Sperry Ethan Matassa Danilo S Stajic Natasa Bogdanovic Radovan M de Blaauw Ivo Marcelis Carlo LM Wijers Charlotte HW Bartels Enrika Schmiedeke Eberhard Schmidt Dominik Maerzheuser Stefanie Grasshoff-Derr Sabine Holland-Cunz Stefan Ludwig Michael Noethen Markus M Draaken Markus Brosens Erwin Heij Hugo Tibboel Dick Herrmann Bernhard G Solomon Benjamin D de Klein Annelies van Rooij Iris ALM Esposito Franca Reutter Heiko M Hildebrandt Friedhelm
Info	KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1310-1317
Projekat	National Institutes of Health [R01-DK045345, R01-DK088767]; March of Dimes Foundation [6FY11-241]; Division of Intramural Research; National Human Genome Research Institute (NHGRI); National Institutes of Health and Human services; Bundesministerium fur B
Ispravka	Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus

Naslov	A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency (Article)
Autori	Bogdanovic Radovan M Draaken Markus Toromanovic Alma Djordjevic Maja S Stajic Natasa Ludwig Michael
Info	PEDIATRIC NEPHROLOGY, (2010), vol. 25 br. 11, str. 2363-2368
Projekat	Ministry of Science, Republic of Serbia [145046D]
Ispravka	Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus

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