Associated Papers
Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria.
Symoens S et al.
Human Mutation, 2012
Molecular genetics in classic Ehlers-Danlos syndrome.
Malfait F et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2005
The molecular basis of classic Ehlers-Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients.
Malfait F et al.
Human Mutation, 2005
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