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Identification and characterization of exonic variants related with familial essential tremor
(Bilkent University, 2017-07)
Essential tremor (ET) is the most common movement disorder in humans. Despite its high heritability and frequency, the genetic basis and pathophysiology of ET is not well understood. In this study, whole exome sequencing ...
Identification of candidate genes for familial essential tremor
(Bilkent University, 2016-09)
Essential tremor (ET) is one of the most common movement disorders in humans and is characterized by action tremors that occur during voluntary motion. However, due to the strong heterogeneity exhibited by ET patients at ...