Results
|
521.
|
|
|
522.
|
|
|
523.
|
|
|
524.
|
|
|
525.
|
|
|
526.
|
|
|
527.
|
|
|
528.
|
ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan. [electronic resource] by
- Gerin, Isabelle
- Ury, Benoît
- Breloy, Isabelle
- Bouchet-Seraphin, Céline
- Bolsée, Jennifer
- Halbout, Mathias
- Graff, Julie
- Vertommen, Didier
- Muccioli, Giulio G
- Seta, Nathalie
- Cuisset, Jean-Marie
- Dabaj, Ivana
- Quijano-Roy, Susana
- Grahn, Ammi
- Van Schaftingen, Emile
- Bommer, Guido T
Producer: 20180920
In:
Nature communications vol. 7
Availability: No items available.
|
|
529.
|
|
|
530.
|
|
|
531.
|
|
|
532.
|
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria. [electronic resource] by
- Cagliani, R
- Comi, G P
- Tancredi, L
- Sironi, M
- Fortunato, F
- Giorda, R
- Bardoni, A
- Moggio, M
- Prelle, A
- Bresolin, N
- Scarlato, G
Producer: 20010719
In:
Neuromuscular disorders : NMD vol. 11
Availability: No items available.
|
|
533.
|
Alpha6beta4 integrin and dystroglycan cooperate to stabilize the myelin sheath. [electronic resource] by
- Nodari, Alessandro
- Previtali, Stefano C
- Dati, Gabriele
- Occhi, Simona
- Court, Felipe A
- Colombelli, Cristina
- Zambroni, Desirée
- Dina, Giorgia
- Del Carro, Ubaldo
- Campbell, Kevin P
- Quattrini, Angelo
- Wrabetz, Lawrence
- Feltri, M Laura
Producer: 20080805
In:
The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 28
Availability: No items available.
|
|
534.
|
|
|
535.
|
|
|
536.
|
The ZZ domain of dystrophin in DMD: making sense of missense mutations. [electronic resource] by
- Vulin, Adeline
- Wein, Nicolas
- Strandjord, Dana M
- Johnson, Eric K
- Findlay, Andrew R
- Maiti, Baijayanta
- Howard, Michael T
- Kaminoh, Yuuki J
- Taylor, Laura E
- Simmons, Tabatha R
- Ray, Will C
- Montanaro, Federica
- Ervasti, Jim M
- Flanigan, Kevin M
Producer: 20140807
In:
Human mutation vol. 35
Availability: No items available.
|
|
537.
|
|
|
538.
|
|
|
539.
|
|
|
540.
|
Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation. [electronic resource] by
- Leibovitz, Zvi
- Mandel, Hanna
- Falik-Zaccai, Tzipora C
- Ben Harouch, Shani
- Savitzki, David
- Krajden-Haratz, Karina
- Gindes, Liat
- Tamarkin, Mordechai
- Lev, Dorit
- Dobyns, William B
- Lerman-Sagie, Tally
Producer: 20180821
In:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 22
Availability: No items available.
|