M. Wagner Et Al. , "Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy," United Kingdom Neuromuscular Translational Research Conference , vol.22, Newcastle-Upon-Tyne, United Kingdom, 2012
Wagner, M. Et Al. 2012. Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy. United Kingdom Neuromuscular Translational Research Conference , (Newcastle-Upon-Tyne, United Kingdom).
Wagner, M., Laval, S., Mueller, J., Durmus, H., Serdaroglu-Oflazer, P., & Lochmueller, H., (2012). Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy . United Kingdom Neuromuscular Translational Research Conference, Newcastle-Upon-Tyne, United Kingdom
Wagner, M. Et Al. "Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy," United Kingdom Neuromuscular Translational Research Conference, Newcastle-Upon-Tyne, United Kingdom, 2012
Wagner, M. Et Al. "Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy." United Kingdom Neuromuscular Translational Research Conference , Newcastle-Upon-Tyne, United Kingdom, 2012
Wagner, M. Et Al. (2012) . "Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy." United Kingdom Neuromuscular Translational Research Conference , Newcastle-Upon-Tyne, United Kingdom.
@conferencepaper{conferencepaper, author={M. Wagner Et Al. }, title={Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy}, congress name={United Kingdom Neuromuscular Translational Research Conference}, city={Newcastle-Upon-Tyne}, country={United Kingdom}, year={2012}}