The elusive Angelman syndrome critical region.

Author:

Trent R J,Sheffield L J,Deng Z M,Kim W S,Nassif N T,Ryce C,Woods C G,Michaelis R C,Tarleton J,Smith A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. American Society of Human Genetics/American College of Medical Genetics Test and Technology Transfer Committee. Diagnostic testing for Prader-Willi and Angelman sydndromes: report of the ASHG/ACMG test and technology transfer committee;Am Hum Genet,1996

2. UBE3A/E6-AP mutations cause Angelman syndrome;Kishino, T.; Lalande, M.; Wagstaff, J.;Nat Genet,1997

3. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome;Matsuura, T.; Sutcliffe, J.S.; Fang, P.;Nat Genet,1997

4. The ubiquitin-proteasome proteolytic pathway;Ciechanover, A.;Cell,1994

5. Deletion involving D 15S 113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region;Michaelis, R.C.; Skinner, S.A.; Lethco, B.A.;Am Med Genet,1995

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The behavioural phenotype of Angelman syndrome;Journal of Intellectual Disability Research;2006-01

2. Imprinting in Angelman and Prader-Willi syndromes;Current Opinion in Genetics & Development;1998-06

3. UBE3A "mutations" in two unrelated and phenotypically different Angelman syndrome patients;Human Genetics;1998-04-23

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