Carrier detection in Duchenne muscular dystrophy using molecular methods

BACKGROUND & OBJECTIVES: Duchenne and Becker muscular dystrophies are X-linked allelic disorders which are caused by mutations in the DMD gene. Carrier analysis in DMD is complicated due to the heterozygous nature of the X chromosome. Several techniques have been tried for carrier analysis in fa...

Descripción completa

Detalles Bibliográficos
Autores principales: Sakthivel Murugan, S.M., Arthi, C., Thilothammal, N., Lakshmi, B.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734715/
https://www.ncbi.nlm.nih.gov/pubmed/23852291

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734715/
https://www.ncbi.nlm.nih.gov/pubmed/23852291

Ejemplares similares