Results
|
|
141.
|
A new mutation of the SCGA gene is the cause of a late onset mild phenotype limb girdle muscular dystrophy type 2D with axial involvement. [electronic resource] by
- Gonzalez-Quereda, Lidia
- Gallardo, Eduard
- Töpf, Ana
- Alonso-Jimenez, Alicia
- Straub, Volker
- Rodriguez, Maria Jose
- Lleixa, Cinta
- Illa, Isabel
- Gallano, Pia
- Diaz-Manera, Jordi
Producer: 20191023
In:
Neuromuscular disorders : NMD vol. 28
Availability: No items available.
|
|
|
142.
|
|
|
|
143.
|
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias. [electronic resource] by
- Grundmann, Kathrin
- Laubis-Herrmann, Ulrike
- Dressler, Dirk
- Vollmer-Haase, Juliane
- Bauer, Peter
- Stuhrmann, Manfred
- Schulte, Thorsten
- Schöls, Ludger
- Topka, Helge
- Riess, Olaf
Producer: 20050214
In:
Movement disorders : official journal of the Movement Disorder Society vol. 19
Availability: No items available.
|
|
|
144.
|
|
|
|
145.
|
|
|
|
146.
|
|
|
|
147.
|
|
|
|
148.
|
|
|
|
149.
|
miR669a and miR669q prevent skeletal muscle differentiation in postnatal cardiac progenitors. [electronic resource] by
- Crippa, Stefania
- Cassano, Marco
- Messina, Graziella
- Galli, Daniela
- Galvez, Beatriz G
- Curk, Tomaz
- Altomare, Claudia
- Ronzoni, Flavio
- Toelen, Jaan
- Gijsbers, Rik
- Debyser, Zeger
- Janssens, Stefan
- Zupan, Blaz
- Zaza, Antonio
- Cossu, Giulio
- Sampaolesi, Maurilio
Producer: 20110902
In:
The Journal of cell biology vol. 193
Availability: No items available.
|
|
|
150.
|
|
|
|
151.
|
|
|
|
152.
|
|
|
|
153.
|
|
|
|
154.
|
|
|
|
155.
|
|
|
|
156.
|
|
|
|
157.
|
|
|
|
158.
|
Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia. [electronic resource] by
- Gerrits, M C F
- Foncke, E M J
- de Haan, R
- Hedrich, K
- van de Leemput, Y L C
- Baas, F
- Ozelius, L J
- Speelman, J D
- Klein, C
- Tijssen, M A J
Producer: 20060424
In:
Neurology vol. 66
Availability: No items available.
|
|
|
159.
|
|
|
|
160.
|
|