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Cri du chat syndrome patients have DNA methylation changes in genes linked to symptoms of the disease
BACKGROUND: Cri du chat (also called 5p deletion, or monosomy 5p) syndrome is a genetic disease caused by deletions of various lengths in the short (p) arm of chromosome 5. Genetic analysis and phenotyping have been used to suggest dose-sensitive genes in this region that may cause symptoms when a g...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563797/ https://www.ncbi.nlm.nih.gov/pubmed/36242045 http://dx.doi.org/10.1186/s13148-022-01350-3 |