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    TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport von Hou, Yuqing, Boldt, Karsten, van Reeuwijk, Jeroen, Plaza, Jean-Marc, Letteboer, Stef J. F, Johnson, Colin A, Kayserili, Hulya, King, Stephen M, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Anderson, Carl, Ayub, Mohammad, Barroso, Inês, Bentham, Jamie, Bhattacharya, Shoumo, Bochukova, Elena, Bolton, Patrick, Boustred, Chris, Breen, Gerome, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Cirak, Sebhattin, Coates, Guy, Collier, David, Craddock, Nick, Crooks, Lucy, Daly, Allan, Smith, George Davey, Day-Williams, Aaron, Edkins, Sarah, Fitzpatrick, David, Floyd, Jamie, Futema, Marta, Gallagher, Louise, Grozeva, Detelina, Hendricks, Audrey, Holmans, Peter, Humphries, Steve E, Hurles, Matt, Jackson, David, Jamshidi, Yalda, Chris, Joyce, Keane, Thomas, Kennedy, Karen, Kolb-Kokocinski, Anja, Lachance, Genevieve, Lee, Irene, Li, Rui, Ryan, Liu, Lönnqvist, Jouko, Lopes, Margarida, MacArthur, Daniel G, Massimo, Mangino, Marchini, Jonathan, Maslen, John, McKechanie, Andrew, Metrustry, Sarah, Moayyeri, Alireza, Muddyman, Dawn, Muntoni, Francesco, Northstone, Kate, O'Rahilly, Stephen, Onoufriadis, Alexandros, Oualkacha, Karim, Panoutsopoulou, Kalliope, Parr, Jeremy, Paternoster, Lavinia, Paunio, Tiina, Pietilainen, Olli, Plagnol, Vincent, Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Brent Richards, J, Ring, Sue, Ritchie, Graham R S, Serra, Eva, Shin, So-Youn, Small, Kerrin, Soranzo, Nicole, St Pourcain, Beate, St. Clair, David, Surdulescu, Gabriela, Suvisaari, Jaana, Tian, Jing, Timpson, Nic, Valdes, Ana, van Kogelenberg, Margriet, Wang, Jun, Ward, Kirsten, Wheeler, Ellie, Williams, Hywel, Williamson, Kathy, Wilson, Scott G, Whyte, Tamieka, ChangJiang, Xu, Zeggini, Eleftheria


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