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.identifier.uri | http://repository.limu.edu.ly/handle/123456789/300 | |
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.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 |