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	1.	Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling. [electronic resource] by Rice, Gillian I Del Toro Duany, Yoandris Jenkinson, Emma M Forte, Gabriella Ma Anderson, Beverley H Ariaudo, Giada Bader-Meunier, Brigitte Baildam, Eileen M Battini, Roberta Beresford, Michael W Casarano, Manuela Chouchane, Mondher Cimaz, Rolando Collins, Abigail E Cordeiro, Nuno Jv Dale, Russell C Davidson, Joyce E De Waele, Liesbeth Desguerre, Isabelle Faivre, Laurence Fazzi, Elisa Isidor, Bertrand Lagae, Lieven Latchman, Andrew R Lebon, Pierre Li, Chumei Livingston, John H Lourenço, Charles M Mancardi, Maria Margherita Masurel-Paulet, Alice McInnes, Iain B Menezes, Manoj P Mignot, Cyril O'Sullivan, James Orcesi, Simona Picco, Paolo P Riva, Enrica Robinson, Robert A Rodriguez, Diana Salvatici, Elisabetta Scott, Christiaan Szybowska, Marta Tolmie, John L Vanderver, Adeline Vanhulle, Catherine Vieira, Jose Pedro Webb, Kate Whitney, Robyn N Williams, Simon G Wolfe, Lynne A Zuberi, Sameer M Hur, Sun Crow, Yanick J Producer: 20140616 In: Nature genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. [electronic resource] by Crow, Yanick J Chase, Diana S Lowenstein Schmidt, Johanna Szynkiewicz, Marcin Forte, Gabriella M A Gornall, Hannah L Oojageer, Anthony Anderson, Beverley Pizzino, Amy Helman, Guy Abdel-Hamid, Mohamed S Abdel-Salam, Ghada M Ackroyd, Sam Aeby, Alec Agosta, Guillermo Albin, Catherine Allon-Shalev, Stavit Arellano, Montse Ariaudo, Giada Aswani, Vijay Babul-Hirji, Riyana Baildam, Eileen M Bahi-Buisson, Nadia Bailey, Kathryn M Barnerias, Christine Barth, Magalie Battini, Roberta Beresford, Michael W Bernard, Geneviève Bianchi, Marika Billette de Villemeur, Thierry Blair, Edward M Bloom, Miriam Burlina, Alberto B Carpanelli, Maria Luisa Carvalho, Daniel R Castro-Gago, Manuel Cavallini, Anna Cereda, Cristina Chandler, Kate E Chitayat, David A Collins, Abigail E Sierra Corcoles, Concepcion Cordeiro, Nuno J V Crichiutti, Giovanni Dabydeen, Lyvia Dale, Russell C D'Arrigo, Stefano De Goede, Christian G E L De Laet, Corinne De Waele, Liesbeth M H Denzler, Ines Desguerre, Isabelle Devriendt, Koenraad Di Rocco, Maja Fahey, Michael C Fazzi, Elisa Ferrie, Colin D Figueiredo, António Gener, Blanca Goizet, Cyril Gowrinathan, Nirmala R Gowrishankar, Kalpana Hanrahan, Donncha Isidor, Bertrand Kara, Bülent Khan, Nasaim King, Mary D Kirk, Edwin P Kumar, Ram Lagae, Lieven Landrieu, Pierre Lauffer, Heinz Laugel, Vincent La Piana, Roberta Lim, Ming J Lin, Jean-Pierre S-M Linnankivi, Tarja Mackay, Mark T Marom, Daphna R Marques Lourenço, Charles McKee, Shane A Moroni, Isabella Morton, Jenny E V Moutard, Marie-Laure Murray, Kevin Nabbout, Rima Nampoothiri, Sheela Nunez-Enamorado, Noemi Oades, Patrick J Olivieri, Ivana Ostergaard, John R Pérez-Dueñas, Belén Prendiville, Julie S Ramesh, Venkateswaran Rasmussen, Magnhild Régal, Luc Ricci, Federica Rio, Marlène Rodriguez, Diana Roubertie, Agathe Salvatici, Elisabetta Segers, Karin A Sinha, Gyanranjan P Soler, Doriette Spiegel, Ronen Stödberg, Tommy I Straussberg, Rachel Swoboda, Kathryn J Suri, Mohnish Tacke, Uta Tan, Tiong Y te Water Naude, Johann Wee Teik, Keng Thomas, Maya Mary Till, Marianne Tonduti, Davide Valente, Enza Maria Van Coster, Rudy Noel van der Knaap, Marjo S Vassallo, Grace Vijzelaar, Raymon Vogt, Julie Wallace, Geoffrey B Wassmer, Evangeline Webb, Hannah J Whitehouse, William P Whitney, Robyn N Zaki, Maha S Zuberi, Sameer M Livingston, John H Rozenberg, Flore Lebon, Pierre Vanderver, Adeline Orcesi, Simona Rice, Gillian I Producer: 20150916 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)