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Epigenomic Approaches for the Diagnosis of Rare Diseases
Rare diseases affect more than 300 million people worldwide. Diagnosing rare diseases is a major challenge as they have different causes and etiologies. Careful assessment of clinical symptoms often leads to the testing of the most common genetic alterations that could explain the disease. Patients...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9397041/ https://www.ncbi.nlm.nih.gov/pubmed/35997367 http://dx.doi.org/10.3390/epigenomes6030021 |