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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...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC425576/ https://ncbi.nlm.nih.gov/pubmed/15175115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-5-13 |
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