Matrilineal analysis of mutations in the DMD gene in a multigenerational South Indian cohort using DMD gene panel sequencing

Author:

Shastry Arun1,Aravind Sankaramoorthy12,Sunil Meeta3,Ramesh Keerthi1,Ashley Berty1,T. Nithyanandan3,Ramprasad Vedam L.3ORCID,Gupta Ravi3,Seshagiri Somasekar4,Nongthomba Upendra2,Phalke Sameer35ORCID

Affiliation:

1. Dystrophy Annihilation Research Trust (DART) Bangalore India

2. Indian Institute of Science (IISc) Bangalore India

3. MedGenome Labs Bangalore India

4. SciGenom Research Foundation Cochin India

5. SciGenom Labs Pvt Ltd Cochin India

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Reference69 articles.

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2. Theoretic applicability of antisense‐mediated exon skipping for Duchenne muscular dystrophy mutations;Aartsma‐Rus A.;Human Mutation,2009

3. The importance of genetic diagnosis for Duchenne muscular dystrophy;Aartsma‐rus A.;Journal of Medical Genetics,2016

4. The genetic status of mothers of isolated cases of Duchenne muscular dystrophy;Aartsma‐Rus A.;Human Genetics,2012

5. Entries in the Leiden Duchenne muscular dystrophy mutation database: An overview of mutation types and paradoxical cases that confirm the reading‐frame rule;Aartsma‐Rus A.;Muscle and Nerve,2006

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