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Browsing publications by
Dr Hacer Durmus.
Newcastle Authors
Title
Year
Full text
Dr Ana Topf
Dr Katherine Johnson
Adam Bates
Lauren Charlotte Phillips Phillips
Dr Marta Bertoli
et al.
Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
2020
Matias Wagner
Dr Steven Laval
Dr Juliane Mueller
Dr Hacer Durmus
Professor Hanns Lochmuller
et al.
Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy
2012
Dr Hacer Durmus
Dr Steven Laval
Professor Volker Straub
Emerita Professor Katherine Bushby
Professor Hanns Lochmuller
et al.
Oculopharyngodistal myopathy is a distinct entity Clinical and genetic features of 47 patients
2011
Dr Hacer Durmus
Dr Juliane Mueller
Professor Hanns Lochmuller
Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations
2010