Mutations in the KMT2B gene have been identified in patients previously diagnosed with idiopathic dystonia. Literature on KMT2B-related dystonia is sparse in the Indian and Asian populations.
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https://www.riss.kr/link?id=A108946664
Debjyoti Dhar (Department of Neurology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India) ; Pramod Kumar Pal (National Institute of Mental Health & Neurosciences)
2023
English
KCI등재,SCOPUS,SCIE
학술저널
285-294(10쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Mutations in the KMT2B gene have been identified in patients previously diagnosed with idiopathic dystonia. Literature on KMT2B-related dystonia is sparse in the Indian and Asian populations.
Mutations in the KMT2B gene have been identified in patients previously diagnosed with idiopathic dystonia. Literature on KMT2B-related dystonia is sparse in the Indian and Asian populations.
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