Identification of Novel KMT2B Variants in Chinese Dystonia Patients via Whole-Exome Sequencing
Background: Dystonia is a movement disorder with high clinical and genetic heterogeneity. Recently mutations in lysine-specific histone methyltransferase 2B (KMT2B) gene have been reported to be associated with early-onset progressive dystonia.Methods: We performed whole-exome sequencings (WES) in a...
I tiakina i:
| Ngā kaituhi matua: | , , , , |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Frontiers Media S.A.
2019-07-01
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| Rangatū: | Frontiers in Neurology |
| Ngā marau: | |
| Urunga tuihono: | https://www.frontiersin.org/article/10.3389/fneur.2019.00729/full |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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