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Kagami–Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region

Human chromosome 14q32.2 carries paternally expressed genes including DLK1 and RTL1, and maternally expressed genes including MEG3 and RTL1as, along with the germline-derived DLK1-MEG3 intergenic differentially methylated region (IG-DMR) and the postfertilization-derived MEG3-DMR. Consistent with th...

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Dades bibliogràfiques
Publicat a:J Hum Genet
Autors principals: Ogata, Tsutomu, Kagami, Masayo
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2016
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4771937/
https://ncbi.nlm.nih.gov/pubmed/26377239
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2015.113
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