F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis

Diverse DNA structural variations (SVs) in human cancers and several other diseases are well documented. For genomic inversions in particular, the disease causing mechanism may not be clear, especially if the inversion border does not cross a coding sequence. Understanding about the molecular proces...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Jamil, Muhammad Ahmer, Sharma, Amit, Nuesgen, Nicole, Pezeshkpoor, Behnaz, Heimbach, André, Pavlova, Anne, Oldenburg, Johannes, El-Maarri, Osman
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6548806/
https://ncbi.nlm.nih.gov/pubmed/31191618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00508
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