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Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

dc.contributor.authorMueller, J.
dc.contributor.authorSerdaroglu-Oflazer, P.
dc.contributor.authorLaval, S.
dc.contributor.authorLochmueller, H.
dc.contributor.authorDurmus, Hacer
dc.contributor.authorWagner, M.
dc.date.accessioned2021-03-05T07:49:11Z
dc.date.available2021-03-05T07:49:11Z
dc.identifier.citationWagner M., Laval S., Mueller J., Durmus H., Serdaroglu-Oflazer P., Lochmueller H., "Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy", United Kingdom Neuromuscular Translational Research Conference, Newcastle-Upon-Tyne, İngiltere, 22 - 23 Mart 2012, cilt.22
dc.identifier.othervv_1032021
dc.identifier.otherav_95b627ac-df0a-4c19-ba80-365dc3881cc0
dc.identifier.urihttp://hdl.handle.net/20.500.12627/100819
dc.language.isoeng
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectTemel Bilimler
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleUsing whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy
dc.typeBildiri
dc.contributor.departmentNewcastle University - UK , ,
dc.identifier.volume22
dc.contributor.firstauthorID139364


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