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Gender influences monoallelic expression of ATP10A in human brain
Human chromosome 15q11-13 and the syntenic region of mouse chromosome 7 contain multiple imprinted genes necessary for proper neurodevelopment. Due to imprinting, paternal 15q11-13 deficiencies lead to Prader-Willi syndrome (PWS) while maternal 15q11-13 deficiencies cause Angelman syndrome (AS). The...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2830741/ https://ncbi.nlm.nih.gov/pubmed/18726118 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-008-0546-0 |
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