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TMEM151A-related Paroxysmal Kinesigenic Dyskinesia in first two Indian families
Revathi Sampath1, Prabhakara Somanna1, Anbazhagan Kolandaswamy2
1Department of Biotechnology, Dr.M.G.R. Educational and Research Institute, Chennai, India; Department of Genetics, RajaRajeswari Medical College and Hospital, Bangalore, India.
Abstract:
The pathogenic variants of TMEM151A are known to be the genetic cause for Paroxysmal Kinesigenic Dyskinesia apart from PRRT2 variants. Through whole exome sequencing, we identified a known variant (c.368G > C; p. Arg123Pro) in the affected siblings of family-1 and a novel heterozygous variant (c.335T > C; p. Leu112Pro) in the patient of family-2.
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