Molecular Diagnosis of Muscular Dystrophy Patients in Western Indian Population: A Comprehensive Mutation Analysis Using Amplicon Sequencing

Muscular Dystrophies (MDs) are a group of inherited diseases and heterogeneous in nature. To date, 40 different genes have been reported for the occurrence and/or progression of MDs. This study was conducted to demonstrate the application of next-generation sequencing (NGS) in developing a time-savi...

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Detalles Bibliográficos
Autores principales: Patel, Komal M., Bhatt, Arpan D., Shah, Krati, Waghela, Bhargav N., Pandit, Ramesh J., Sheth, Harsh, Joshi, Chaitanya G., Joshi, Madhvi N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679082/
https://www.ncbi.nlm.nih.gov/pubmed/34925456
http://dx.doi.org/10.3389/fgene.2021.770350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679082/
https://www.ncbi.nlm.nih.gov/pubmed/34925456
http://dx.doi.org/10.3389/fgene.2021.770350

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