Whole-Exome Sequencing Identifies Small Mutations in Pakistani Muscular Dystrophy Patients-Reference-Cited by-同舟云学术

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Whole-Exome Sequencing Identifies Small Mutations in Pakistani Muscular Dystrophy Patients

Published:2021-03-01 Issue:3 Volume:25 Page:218-226
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Zehravi Mehwish¹,Wahid Mohsin¹²,Ashraf Junaid³,Fatima Tehseen¹⁴

Affiliation:

1. Dow Research Institute of Biotechnology and Biomedical Sciences, Dow University of Health Sciences, Karachi, Pakistan.

2. Department of Pathology, Dow International Medical College, Dow University of Health Sciences, Karachi, Pakistan.

3. Department of Neurosurgery, Dow University of Health Sciences, Karachi, Pakistan.

4. Dow College of Biotechnology, Dow University of Health Sciences, Karachi, Pakistan.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2020.0246

Reference19 articles.

1. The 10th Oligonucleotide Therapy Approved: Golodirsen for Duchenne Muscular Dystrophy

2. The importance of genetic diagnosis for Duchenne muscular dystrophy

3. FDA Approves Eteplirsen for Duchenne Muscular Dystrophy: The Next Chapter in the Eteplirsen Saga

4. MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study

5. The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations

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