Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes

Author:

Baker Emma K.ORCID,Godler David E.,Bui Minh,Hickerton Chriselle,Rogers Carolyn,Field Mike,Amor David J.,Bretherton Lesley

Funder

National Health and Medical Research Council

The Foundation for Prader-Willi Syndrome Research (USA)

Prader-Willi Syndrome Association (Australia)

Foundation for Angelman Syndrome Therapeutics

Dup15q Australia Ltd

Murdoch Children's Research Institute

Medical Research Future Fund

Financial Markets Foundation for Children

Genetics of Learning Disability (GOLD) Service

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Neurology (clinical),Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Reference41 articles.

1. Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Prader-Willi syndrome. Genet Med. 2012;14:10–26.

2. Buiting K, Williams C, Horsthemke B. Angelman syndrome – insights into a rare neurogenetic disorder. Nat Rev Neurol. 2016;12:584–93.

3. Dagli AI, Mueller J, Williams CA. Angelman syndrome. 1998 Sep 15 [updated 2017 Dec 21]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1144/

4. Driscoll DJ, Miller JL, Schwartz S, Cassidy SB. Prader-Willi syndrome. 2016.

5. Nazlican H, Zeschnigk M, Claussen U, Michel S, Boehringer S, Gillessen-Kaesbach G, Buiting K, Horsthemke B. Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Hum Mol Gen. 2004;13:2547–55.

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