Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci
Congenital imprinting disorders (IDs) are characterised by molecular changes affecting imprinted chromosomal regions and genes, i.e. genes that are expressed in a parent-of-origin specific manner. Recent years have seen a great expansion in the range of alterations in regulation, dosage or DNA seque...
| Main Authors: | , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
2015-11-14.
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| Subjects: | |
| Online Access: | Get fulltext |