DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore Sequencing

The molecular genetic mechanism of Turner syndrome (TS) still leaves much to be discovered. Methods: TS (45X0) patients and age-matched controls (46XX and 46XY) were selected. The nanopore sequencing combined with trio-whole exome sequencing (trio-WES) were used for the first time to investigate TS....

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Detalles Bibliográficos
Autores principales: Fan, Xin, Zhang, Beibei, Fan, Lijun, Chen, Jiajia, Su, Chang, Cao, Bingyan, Wei, Liya, Qin, Miao, Gong, Chunxiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225209/
https://www.ncbi.nlm.nih.gov/pubmed/35743657
http://dx.doi.org/10.3390/jpm12060872

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225209/
https://www.ncbi.nlm.nih.gov/pubmed/35743657
http://dx.doi.org/10.3390/jpm12060872

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