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Imprinted expression of SNRPN in human preimplantation embryos.

Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are two clinically distinct neurogenetic disorders arising from a loss of expression of imprinted genes within the human chromosome region 15q11-q13. Recent evidence suggests that the SNRPN gene, which is defective in PWS, plays a central role i...

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Detalhes bibliográficos
Main Authors: Huntriss, J, Daniels, R, Bolton, V, Monk, M
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377472/
https://ncbi.nlm.nih.gov/pubmed/9758597
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