Paternal imprinting of the <it>SLC22A1LS </it>gene located in the human chromosome segment 11p15.5
<p>Abstract</p> <p>Background</p> <p>Genomic imprinting is an epigenetic chromosomal modification in the gametes or zygotes that results in a non-random monoallelic expression of specific autosomal genes depending upon their parent of origin. Approximately 44 human gene...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2004-06-01
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| Series: | BMC Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2156/5/13 |