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Recurrent pneumothorax in a case of tenascin‐X deficient Ehlers–Danlos syndrome: Broadening the phenotypic spectrum
The genomic region surrounding the Tenascin‐XB gene ( TNXB ) is a complex and duplicated region, with several pseudogenes that predispose to high rates of homologous recombination. Classical‐like Ehlers–Danlos syndrome (clEDS) is the result of tenascin‐X deficiency due to biallelic loss of function...
Autores principales: | Santoreneos, Renee, Vakulin, Cassandra, Ellul, Melissa, Rawlings, Lesley, Hardy, Tristan, Poplawski, Nicola |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9303620/ https://www.ncbi.nlm.nih.gov/pubmed/35128805 http://dx.doi.org/10.1002/ajmg.a.62674 |
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