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"Roote, G T" » "Route, G T"
"Roote, G T" » "Route, G T"
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum
Serpieri, Valentina, D’Abrusco, Fulvio, Dempsey, Jennifer C, Cheng, Yong-Han Hank, Arrigoni, Filippo, Baker, Janice, Battini, Roberta, Bertini, Enrico Silvio, Borgatti, Renato, Christman, Angela K, Curry, Cynthia, D'Arrigo, Stefano, Fluss, Joel, Freilinger, Michael, Gana, Simone, Ishak, Gisele E, Leuzzi, Vincenzo, Loucks, Hailey, Manti, Filippo, Mendelsohn, Nancy, Merlini, Laura, Miller, Caitlin V, Muhammad, Ansar, Nuovo, Sara, Romaniello, Romina, Schmidt, Wolfgang, Signorini, Sabrina, Siliquini, Sabrina, Szczałuba, Krzysztof, Vasco, Gessica, Wilson, Meredith, Zanni, Ginevra, Boltshauser, Eugen, Doherty, Dan, Valente, Enza Maria, Bamshad, M J, Leal, S M, Nickerson, D A, Anderson, P, Bacus, T J, Blue, E E, Brower, K, Buckingham, K J, Chong, J X, Cornejo Sánchez, D, Davis, C P, Davis, C J, Frazar, C D, Gomeztagle-Burgess, K, Gordon, W W, Horike-Pyne, M, Hurless, J R, Jarvik, G P, Johanson, E, Kolar, J T, Marvin, C T, McGee, S, McGoldrick, D J, Mekonnen, B, Nielsen, P M, Patterson, K, Radhakrishnan, A, Richardson, M A, Roote, G T, Ryke, E L, Schrauwen, I, Shively, K M, Smith, J D, Tackett, M, Wang, G, Weiss, J M, Wheeler, M M, Yi, Q, Zhang, X
Published in Journal of medical genetics (01.09.2022)
Published in Journal of medical genetics (01.09.2022)
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