Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction.

Kolvenbach, Caroline M; Dworschak, Gabriel C; Frese, Sandra; Japp, Anna S; Schuster, Peggy; Wenzlitschke, Nina; Yilmaz, Öznur; Lopes, Filipa M; Pryalukhin, Alexey; Schierbaum, Luca; van der Zanden, Loes F M; Kause, Franziska; Schneider, Ronen; Taranta-Janusz, Katarzyna; Szczepanska, Maria; Pawlaczyk, Krzysztof; Newman, William G; Beaman, Glenda M; Stuart, Helen M; Cervellione, Raimondo M; Feitz, Wouter F J; van Rooij, Iris A L M; Schreuder, Michiel F; Steffens, Martijn; Weber, Stefanie; Merz, Waltraut M; Feldkötter, Markus; Hoppe, Bernd; Thiele, Holger; Altmüller, Janine; Berg, Christoph; Kristiansen, Glen; Ludwig, Michael; Reutter, Heiko; Woolf, Adrian S; Hildebrandt, Friedhelm; Grote, Phillip; Zaniew, Marcin; Odermatt, Benjamin; Hilger, Alina C.
Am J Hum Genet; 104(5): 994-1006, 2019 05 02.
Artigo em Inglês | MEDLINE | ID: mdl-31051115

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