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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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Cold Spring Harbor Laboratory Press 1997
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC139148/
https://ncbi.nlm.nih.gov/pubmed/9110176
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