Congenital imprinting disorders: application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management
Imprinting disorders (IDs) are a group of congenital diseases affecting growth, development and metabolism. They are caused by changes in the allele-specific regulation ("epigenetic mutation") or in the genomic sequence ("genetic mutation") of imprinted genes. Currently molecular...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
2015-10.
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| Subjects: | |
| Online Access: | Get fulltext |