The E6–AP Ubiquitin–Protein Ligase (UBE3A) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region

Angelman syndrome (AS) and Prader–Willi syndrome (PWS) are distinct clinical phenotypes resulting from maternal and paternal deficiencies, respectively, in human chromosome 15q11–q13. Although several imprinted, paternally expressed transcripts have been identified within the PWS candidate region, n...

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Autors principals: Sutcliffe, James S., Jiang, Yong-hui, Galjaard, Robert-Jan, Matsuura, Toshinobu, Fang, Ping, Kubota, Takeo, Christian, Susan L., Bressler, Jan, Cattanach, Bruce, Ledbetter, David H., Beaudet, Arthur L.
Format: Artigo
Idioma:Inglês
Publicat: Cold Spring Harbor Laboratory Press 1997
Matèries:
Letters
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC139148/
https://ncbi.nlm.nih.gov/pubmed/9110176
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