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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Cold Spring Harbor Laboratory Press 1997
Pynciau:
Letters
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC139148/
https://ncbi.nlm.nih.gov/pubmed/9110176
Tagiau: Ychwanegu Tag
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