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Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family

Joint hypermobility is a common, mostly benign, finding in the general population. In a subset of individuals, however, it causes a range of clinical problems, mainly affecting the musculoskeletal system. Joint hypermobility often appears as a familial trait and is shared by several heritable connec...

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Bibliografiska uppgifter
I publikationen:Dis Markers
Huvudupphovsmän: Syx, Delfien, Symoens, Sofie, Steyaert, Wouter, De Paepe, Anne, Coucke, Paul J., Malfait, Fransiska
Materialtyp: Artigo
Språk:Inglês
Publicerad: Hindawi Publishing Corporation 2015
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4609397/
https://ncbi.nlm.nih.gov/pubmed/26504261
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/828970
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