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LGMD2E is the most common type of sarcoglycanopathies in the Iranian population. [electronic resource] by
- Alavi, Afagh
- Esmaeili, Sara
- Nilipour, Yalda
- Nafissi, Shahriar
- Tonekaboni, Seyed Hasan
- Zamani, Gholamreza
- Ashrafi, Mahmoud Reza
- Kahrizi, Kimia
- Najmabadi, Hossein
- Jazayeri, Fatemeh
Producer: 20180510
In:
Journal of neurogenetics vol. 31
Availability: No items available.
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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.
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Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2D. [electronic resource] by
- Fayssoil, Abdallah
- Ogna, Adam
- Chaffaut, Cendrine
- Chevret, Sylvie
- Guimarães-Costa, Raquel
- Leturcq, France
- Wahbi, Karim
- Prigent, Helene
- Lofaso, Frederic
- Nardi, Olivier
- Clair, Bernard
- Behin, Anthony
- Stojkovic, Tanya
- Laforet, Pascal
- Orlikowski, David
- Annane, Djillali
Producer: 20170217
In:
PloS one vol. 11
Availability: No items available.
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