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Severe phenotypes of B3GAT3-related disorder caused by two heterozygous variants: a case report and literature review
BACKGROUND: Linkeropathies refers to a series of extremely rare hereditary connective tissue diseases affected by various glycosyltransferases in the biosynthesis of proteoglycans. We report for the first time two heterozygous variants of B3GAT3 in a Chinese infant, in whom Marfan syndrome was suspe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841085/ https://www.ncbi.nlm.nih.gov/pubmed/35151321 http://dx.doi.org/10.1186/s12920-022-01160-9 |