Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients-Reference-Cited by-同舟云学术

Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients

Published:2016-11-04 Issue:3 Volume:91 Page:411-425
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Demirdas S.¹²,Dulfer E.³,Robert L.⁴,Kempers M.²,van Beek D.⁵,Micha D.⁵,van Engelen B.G.⁶,Hamel B.²,Schalkwijk J.⁶,Loeys B.²⁷,Maugeri A.⁵,Voermans N.C.⁸

Affiliation:

1. Department of Clinical GeneticsErasmus Medical Centre Rotterdam the Netherlands

2. Department of Human GeneticsRadboud University Medical Centre Nijmegen the Netherlands

3. Department of GeneticsUniversity Medical Centre Groningen Groningen the Netherlands

4. Department of GeneticsGuy's and St Thomas' Hospital London UK

5. Department of Clinical Genetics, Centre for Connective Tissue ResearchVU University Medical Centre Amsterdam the Netherlands

6. Department of DermatologyRadboud University Medical Centre Nijmegen the Netherlands

7. Centre for Medical GeneticsUniversity Hospital of Antwerp/University of Antwerp Antwerp Belgium

8. Department of NeurologyRadboud University Medical Centre Nijmegen the Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.12853

Reference22 articles.

1. Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997

2. Tenascin–X deficiency is associated with Ehlers–Danlos syndrome

3. A Recessive Form of the Ehlers–Danlos Syndrome Caused by Tenascin-X Deficiency

4. A clinical and cardiovascular survey of Ehlers‐Danlos syndrome patients with complete deficiency of tenascin‐X;Peeters AC;Neth J Med,2004

5. Tenascin-X deficiency in autosomal recessive Ehlers-Danlos syndrome

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