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Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5
BACKGROUND: 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 genes have been reported to be imprinted. A majority of the...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2004
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC425576/ https://www.ncbi.nlm.nih.gov/pubmed/15175115 http://dx.doi.org/10.1186/1471-2156-5-13 |