...GNAL (DYT25), and TUBB4A (DYT4). Despite these advances, major gaps remain in identifying the genetic origins for most c...
...GNAL, SPOCK3, ANXA10, HELIOS, MYLK, CCDC14, SPAG9, SOX5, VSNL1, SMC6, GEN1, MSGN1 and ZPAX) may be important for abdomin...
GNAL mutations have been shown to cause adult-onset isolated dystonia, a disabling movement disorder characterized by in...
...GNAL have recently been identified as responsible for primary dystonia, however, GNAL mutations in Chinese patients with...
...GNAL) have made their appearance in the literature. New subtypes of neuronal brain iron accumulation have been delineate...
...GNAL dystonia gene is central for striatal responses to dopamine (DA) and is a component of a molecular pathway already ...
...GNAL variants were present.,GNAL variants seem to be a rare cause of PTD in our mainly sporadic German sample. Low frequ...
...GNAL, and TUBB4A). This progress was primarily achieved because of the application of a new technology, next-generation ...
...GNAL (DYT25). Combined dystonias (with parkinsonism or myoclonus) are further subdivided into persistent (GCHI [DYT5], S...
...GNAL (DYT25). Combined dystonias (with parkinsonism or myoclonus) are further subdivided into persistent (TAF1 [DYT3], G...
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