Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice-Reference-Cited by-同舟云学术

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Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice

Published:2017-08-16 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Born Heather A.,Dao An T.,Levine Amber T.,Lee Wai Ling,Mehta Natasha M.,Mehra Shubhangi,Weeber Edwin J.,Anderson Anne E.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-08825-x.pdf

Reference47 articles.

1. Laan, L. A., v Haeringen, A. & Brouwer, O. F. Angelman syndrome: a review of clinical and genetic aspects. Clin. Neurol. Neurosurg. 101, 161–70 (1999).

2. Clayton-Smith, J. & Laan, L. Angelman syndrome: a review of the clinical and genetic aspects. J. Med. Genet. 40, 87–95 (2003).

3. Smith, J. C., Webb, T., Pembrey, M. E., Nichols, M. & Malcolm, S. Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome. Hum. Genet. 88, 376–8 (1992).

4. Pembrey, M. et al. The association of Angelman’s syndrome with deletions within 15q11-13. J. Med. Genet. 26, 73–7 (1989).

5. Laan, L. A. et al. Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated cases. Am. J. Med. Genet. 76, 262–8 (1998).

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