Immunofluorescence microscopy (IFM) analysis of primary ciliary dyskinesia (PCD) patients with suspected inner dynein arm defects (IDA)

Por Hjeij, R, Loges, NT, Becker-Heck, A, Omran, H
Publicado em 2012

Mutations in CCDC39 and CCDC40 are a major cause of primary ciliary dyskinesia with microtubule disorganisation

Por Antony, D, Becker-Heck, A, Forouhan, M, Schmidts, M, Onoufriadis, A, Shoemark, A, Dixon, M, Jackson, C, Goggin, P, Olbrich, H, O’Callaghan, C, Lucas, J, Hogg, C, Chung, EMK, Omran, H, Mitchison, HM
Publicado em 2012

Identification of human mutations in TRAF3IP1 in patients with nephronophthisis and retinal degeneration

Por Becker-Heck, A, Bizet, A, Ryan, R, Krug, P, Filhol, E, Linghu, B, Oakeley, E, Serluca, F, Legendre, F, Dörner, N, Lasbennes, MC, Duca, J, Yang, F, Damask, A, Klickstein, L, Labow, M, Schebesta, M, Bouwmeester, T, Valette, H, Pinson, L, Goubaux, B, Dubot, P, Salomon, R, Antignac, C, Gubler, M, Jeanpierre, C, Chibout, S, Bole-Feysot, C, Nitschké, P, Benmerah, A, Szustakowski, JD, Sailer, AW, Saunier, S, Saint-Mezard, P
Publicado no Cilia (2015)