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: | Soellner, Lukas (Author), Monk, David (Author), Rezwan, Faisal I. (Author), Begemann, Matthias (Author), Mackay, Deborah (Author), Eggermann, Thomas (Author) |
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Format: | Article |
Language: | English |
Published: |
2015-10.
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Subjects: | |
Online Access: | Get fulltext |
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