Use este identificador para citar ou linkar para este item:
https://hdl.handle.net/20.500.12394/7600
Título: | Biochemistry, cytogenetics and DMD gene mutations in South Indian patients with duchenne muscular dystrophy |
Autor(es): | Meyyazhagan, A. Raman, N. M. Easwaran, M Balasubramanian, B Alagamuthu, K. Bhotla, H. Kuchi Shanmugam, S. Inbaraj, K. Kumar, M. Ramesh Kumar, P. Thangamani, L. Piramanayagam, S. Anand, V. Mohd, Y. Park, S. Teijido, O. Carril, J. C. Cacabelos, P. Keshavarao, S. Cacabelos, R. |
Palavras-chave: | Enfermedades musculares Niños Bioquímica médica Citología India |
Editor: | Universidad Continental |
Data do documento: | 2017 |
metadata.dc.date.available: | 7-Jul-2020 |
metadata.dc.date.created: | 2017 |
Citação: | Meyyazhagan, A., Raman, N., Easwaran, M., Balasubramanian, B., Alagamuthu, K., Bhotla, H., Shanmugam, S., Inbaraj, K., Kumar, M., Kumar, P., Thangamani, L., Piramanayagam, S., Anand, V., Mohd, Y., Park, S., Teijido, O., Carril, J., Cacabelos, P., Keshavarao, S., Cacabelos, R. (2017). Biochemistry, cytogenetics and DMD gene mutations in South Indian patients with duchenne muscular dystrophy. International Journal Of Human Genetics, 17(3), 126-134. 10.1080/09723757.2017.1387381 |
metadata.dc.identifier.doi: | 10.1080/09723757.2017.1387381 |
Resumo: | Thirty children aged 3-10 years with clinically confirmed or suspected Duchenne Muscular Dystrophy (DMD) were analyzed for chromosomal aberrations using cytological preparations, biochemical changes using enzyme kit protocol, and deletions in the 26 exons of the DMD gene by targeting the mutations at the proximal and distal ‘hot spot’ regions of the dystrophin gene in South Indian patients with DMD. The frequenc y of chromosomal aberrations (both chromosomal and chromatid-type) and serum enzyme levels were significa ntly elevated in DMD subjects as compared to controls. Multiplex PCR assays revealed 27 patients having deletions in the DMD gene located at the distal ‘hot spot’ region. This study suggests that disease progression is directly associated with higher incidence of the deletions at the distal ‘hot spot’ of the DMD gene. |
metadata.dc.description.note: | El texto completo de este trabajo no está disponible en el Repositorio Institucional - Continental por restricciones de la casa editorial donde ha sido publicado. |
metadata.dc.relation: | https://www.tandfonline.com/doi/abs/10.1080/09723757.2017.1387381 |
Extension: | p. 126-134 |
metadata.dc.rights.accessRights: | Restringido |
metadata.dc.source: | Universidad Continental Repositorio Institucional - Continental |
Aparece nas coleções: | Artículos Científicos |
Arquivos associados a este item:
Não existem arquivos associados a este item.
Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.