Mutations in DSTYK and Dominant Urinary Tract Malformations
Author(s) -
Simone SannaCherchi,
Rosemary V. Sampogna,
Natalia Papeta,
Katherine Burgess,
Shan N. Nees,
Benjamin J. Perry,
Monica Young Choi,
Monica Bodria,
Ying Liu,
Patricia L. Weng,
Vladimir J. Lozanovski,
Miguel Verbitsky,
Francesca Lugani,
Roel Sterken,
Neal Paragas,
Gianluca Caridi,
Alba Carrea,
M. Dagnino,
Anna MaternaKiryluk,
Giuseppe Santamaria,
Corrado Murtas,
Nadica Ristoska-Bojkovska,
Claudia Izzi,
Nilgun Kacak,
B. Bianco,
Stefania Giberti,
Maddalena Gigante,
Giorgio Piaggio,
Loreto Gesualdo,
D. Kosuljandic Vukic,
Katarina Vukojević,
Mirna SaragaBabić,
Marijan Saraga,
Zoran Gucev,
L Allegri,
Anna LatosBieleńska,
D. Casu,
Matthew W. State,
Francesco Scolari,
Roberto Ravazzolo,
Krzysztof Kiryluk,
Qais AlAwqati,
Vivette D. D’Agati,
Iain A. Drummond,
Velibor Tasić,
Richard P. Lifton,
Gian Marco Ghiggeri,
Ali G. Gharavi
Publication year - 2013
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1214479
Subject(s) - medicine , urinary system , kidney , congenital malformations , pathology , bioinformatics , genetics , pregnancy , biology
Congenital abnormalities of the kidney and the urinary tract are the most common cause of pediatric kidney failure. These disorders are highly heterogeneous, and the etiologic factors are poorly understood.
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