Biallelic mutations in Tenascin-X cause classical-like Ehlers-Danlos syndrome with slowly progressive muscular weakness

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Publication year
2020
Author(s)
Brisset, Marion
Metay, Corinne
Carlier, Robert-Yves
Badosa, Carmen
Marques, Caterina
Schalkwijk, J.
Laforet, Pascal
Malfatti, Edoardo
Source
Neuromuscular Disorders, 30, 10, (2020), pp. 833-838
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/226197   https://hdl.handle.net/2066/226197
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