Genes and Pseudogenes: Complexity of the RCCX Locus and Disease
Copy Number Variations (CNVs) account for a large proportion of human genome and are a primary contributor to human phenotypic variation, in addition to being the molecular basis of a wide spectrum of disease. Multiallelic CNVs represent a considerable fraction of large CNVs and are strictly related...
| Published in: | Frontiers in Endocrinology |
|---|---|
| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2021-07-01
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| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2021.709758/full |