Deletion pattern in the dystrophin gene in Duchenne muscular dystrophy patients in northeast India

Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder that affects 1 in 3,500 males and is caused by mutations in the dystrophin gene. In this paper, we have reported DNA analysis of DMD patients by multiplex polymerase chain reaction (PCR) from various states of northeast India. Of th...

Descripción completa

Detalles Bibliográficos
Autores principales: Basumatary, Lakshya J, Das, Marami, Goswami, Munindra, Kayal, Ashok K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724316/
https://www.ncbi.nlm.nih.gov/pubmed/23914114
http://dx.doi.org/10.4103/0976-3147.112777

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724316/
https://www.ncbi.nlm.nih.gov/pubmed/23914114
http://dx.doi.org/10.4103/0976-3147.112777

Ejemplares similares