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Gene therapy for selected neuromuscular and trinucleotide repeat disorders – An insight to subsume South Asia for multicenter clinical trials

Background: In this article, the authors discuss how they utilized the genetic mutation data in Sri Lankan Duchenne muscular dystrophy (DMD), Spinal muscular atrophy (SMA), Spinocerebellar ataxia (SCA) and Huntington’s disease (HD) patients and compare the available literature from South Asian count...

Whakaahuatanga katoa

I tiakina i:
Ngā kaituhi matua: Nalaka Wijekoon, Lakmal Gonawala, Pyara Ratnayake, Darshana Sirisena, Harsha Gunasekara, Athula Dissanayake, Sunethra Senanayake, Ajantha Keshavaraj, Yetrib Hathout, Harry W.M. Steinbusch, Chandra Mohan, Ashwin Dalal, Eric Hoffman, K.Ranil D de Silva
Hōputu: Artigo
Reo:Inglês
I whakaputaina: Elsevier 2023-06-01
Rangatū:IBRO Neuroscience Reports
Ngā marau:
Indian Sub-continent
Developing Countries
Neurogenetic Disorders
Bio Bank
Duchenne Muscular Dystrophy
Spinal Muscular Atrophy
Urunga tuihono:http://www.sciencedirect.com/science/article/pii/S266724212300009X
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