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Case report: further delineation of AEBP1-related Ehlers–Danlos Syndrome (classical-like EDS type 2) in an additional patient and comprehensive clinical and molecular review of the literature
The Ehlers–Danlos Syndromes (EDS), a group of hereditary connective tissue disorders, were classified into 13 subtypes in the 2017 International Classification. Recently, a new subtype of EDS called classical-like EDS type 2 (clEDS2), which is caused by biallelic variants in the adipocyte enhancer b...
Autores principales: | Yamaguchi, Tomomi, Hayashi, Shujiro, Nagai, So, Uchiyama, Akihiko, Motegi, Sei-Ichiro, Fujikawa, Tomomi, Takiguchi, Yuri, Kosho, Tomoki |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196838/ https://www.ncbi.nlm.nih.gov/pubmed/37214418 http://dx.doi.org/10.3389/fgene.2023.1102101 |
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