Genetic basis of Ehlers-Danlos syndrome
| dc.contributor.author | Ibkhatra, Islam Salem | |
| dc.date.accessioned | 2019-02-02T11:20:20Z | |
| dc.date.available | 2019-02-02T11:20:20Z | |
| dc.date.issued | 2018-05-05 | |
| dc.description | In this report, we will discuss the genetic and biochemical data, the current Villefranche classification subdivides EDS into six major subtypes, , which are caused by mutations in genes encoding fibrillar collagens or enzymes involved in collagen biosynthesis. Mutations in type V and type III collagen cause classic and vascular EDS, respectively, whereas mutations affecting the processing of type I collagen lead to the kyphoscoliotic, arthrochalasic and dermatosparactic EDS types | en_US |
| dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/414 | |
| 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 | Genetic basis of Ehlers-Danlos syndrome | en_US |
| dc.title.alternative | (Rubber syndrome) | en_US |
| dc.type | Other | en_US |
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