We Must Accept Finite Disappointment, But Never Lose Infinite Hope
| dc.contributor.author | Al-mogrbi, Hadeel Ahmad | |
| dc.date.accessioned | 2018-06-27T09:46:09Z | |
| dc.date.available | 2018-06-27T09:46:09Z | |
| dc.date.issued | 2018-05-06 | |
| dc.description | Spinal muscular atrophy is a genetic disorder of motor neurons, the cause of most forms of SMA is the deficiency of SMN protein. • full-length,functional SMN protein using genetic instructions carried in the SMN1 gene & identical neighboring gene, called SMN2, typically direct cells to produce a short, partially functional version of the SMN protein. • The great deal of SMA research is aimed at increasing SMN levels, improving muscle strength and function through development of various strategies | en_US |
| dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/300 | |
| dc.language.iso | en | en_US |
| dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
| dc.rights | Attribution 3.0 United States | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
| dc.title | We Must Accept Finite Disappointment, But Never Lose Infinite Hope | en_US |
| dc.title.alternative | Treatment of Spinal muscular atrophy in children | en_US |
| dc.type | Other | en_US |