Logo Logo

Publications by Roos, A.

Up a level
Export as [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | Date
Number of items: 3.

Journal article

Topf, A.; Azuma, Y.; Gorokhova, S.; O'Connor, E.; Porter, A.; Harris, E.; Evangelista, T.; Cox, D.; Lorenzoni, P.; McMacken, G.; Barton, M.; McArthur, D.; Magnusson, O.; Abicht, A.; Senderek, J.; Roos, A.; Abicht, A.; Lochmüller, H. (2017): Next generation sequencing technologies in the genetic diagnosis of congenital myasthenic syndrome. In: Neuromuscular Disorders, Vol. 27: S196-S197

Roos, A.; Senderek, J.; Cox, D.; Wiessner, M.; Zahedi, R.; Charlton, R.; Barresi, R.; Hathazi, D.; Lochmüller, H. (2017): Autosomal recessive myopathy associated with cataracts and learning difficulties caused by INPP5K mutations: a new syndromic gene linking four overlapping rare recessive neuromuscular disorders. In: Neuromuscular Disorders, Vol. 27: S110-S110

Carr, S.; Ritso, M.; Roos, A.; Laval, S.; Krebs, S.; Graf, A.; Blum, H.; Lochmuller, H. (2016): Reversing mdx cardiomyocyte hypertrophy in vitro. In: Neuromuscular Disorders, Vol. 26: S129-S130

This list was generated on Mon Nov 18 06:39:32 2019 CET.