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Genetic basis of Ehlers-Danlos syndrome

dc.contributor.authorIbkhatra, Islam Salem
dc.descriptionIn 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 typesen_US
dc.publisherfaculty of Basic Medical Science - Libyan International Medical Universityen_US
dc.rightsAttribution 3.0 United States*
dc.titleGenetic basis of Ehlers-Danlos syndromeen_US
dc.title.alternative(Rubber syndrome)en_US

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