De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features von Harel, Tamar, Spicher, Camille, Scheer, Elisabeth, Buchan, Jillian G, Cech, Jennifer, Folland, Chiara, Frey, Tanja, Holtz, Alexander M, Innes, A Micheil, Keren, Boris, Macken, William L, Marcelis, Carlo, Otten, Catherine E, Paolucci, Sarah A, Petit, Florence, Pfundt, Rolph, Pitceathly, Robert D S, Rauch, Anita, Ravenscroft, Gianina, Sanchev, Rani, Steindl, Katharina, Tammer, Femke, Tyndall, Amanda, Devys, Didier, Vincent, Stéphane D, Elpeleg, Orly, Tora, László

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De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features: ATXN7L3 variants in developmental delay von Harel, Tamar, Spicher, Camille, Scheer, Elisabeth, Buchan, Jillian, Cech, Jennifer, Folland, Chiara, Frey, Tanja, Holtz, Alexander, Innes, a Micheil, Keren, Boris, Macken, William, Marcelis, Carlo, Otten, Catherine, Paolucci, Sarah, Petit, Florence, Pfundt, Rolph, Pitceathly, Robert, Rauch, Anita, Ravenscroft, Gianina, Sanchev, Rani, Steindl, Katharina, Tammer, Femke, Tyndall, Amanda, Devys, Didier, Vincent, Stéphane D., Elpeleg, Orly, Tora, László

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De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features von Harel, Tamar, Spicher, Camille, Scheer, Elisabeth, Buchan, Jillian G, Cech, Jennifer, Folland, Chiara, Frey, Tanja, Holtz, Alexander M, Innes, A Micheil, Keren, Boris, Macken, William L, Marcelis, Carlo, Otten, Catherine E, Paolucci, Sarah A, Petit, Florence, Pfundt, Rolph, Pitceathly, Robert D S, Rauch, Anita, Ravenscroft, Gianina, Sanchev, Rani, Steindl, Katharina, Tammer, Femke, Tyndall, Amanda, Devys, Didier, Vincent, Stéphane D, Elpeleg, Orly, Tora, László

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