KIAA0586 is mutated in Joubert syndrome

Por Bachmann-Gagescu, Ruxandra, Phelps, Ian G., Dempsey, Jennifer C., Sharma, Vivek A., Ishak, Gisele E., Boyle, Evan A, Wilson, Meredith, Lourenço, Charles Marques, Arslan, Mutluay, Shendure, Jay, Doherty, Dan
Publicado no Hum Mutat (2015)

Further evidence that paroxysmal nocturnal haemoglobinuria is a disorder of defective cell membrane lipid rafts

Por Ratajczak, Mariusz Z, Borkowska, Sylwia, Mierzejewska, Kasia, Kucia, Magda, Mendek-Czajkowska, Ewa, Suszynska, Malwina, Sharma, Vivek A, Deptala, Andrzej, Song, Wechao, Platzbecker, Uwe, Larratt, Loree, Janowska-Wieczorek, Anna, Maciejewski, Jarek, Ratajczak, Janina
Publicado no J Cell Mol Med (2015)