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.identifier.uri	http://repository.limu.edu.ly/handle/123456789/414
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.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

Except where otherwise noted, this item's license is described as Attribution 3.0 United States