The neurobiology of the Prader-Willi phenotype of fragile X syndrome-Reference-Cited by-同舟云学术

The neurobiology of the Prader-Willi phenotype of fragile X syndrome

Published:2016 Issue:4 Volume:5 Page:255-261
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Muzar Zukhrofi¹²,Lozano Reymundo³,Kolevzon Alexander³,Hagerman Randi J.¹

Affiliation:

1. Medical Investigation of Neurodevelopmental Disorders MIND Institute, Department of Pediatrics, UC Davis Medical Center

2. Department of Histology, Universitas Muhammadiyah Sumatera Utara (UMSU) Faculty of Medicine, Medan

3. Seaver Autism Center for Research and Treatment, Departments of Genetics and Genomic Sciences, Psychiatry, and Pediatrics,Icahn School of Medicine at Mount Sinai

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/5/4/5_2016.01082/_pdf

Reference70 articles.

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

3. 3. Butler MG. Prader-Willi Syndrome: Obesity due to genomic imprinting. Curr Genomics. 2011; 12:204-215.

4. 4. Fernández E, Rajan N, Bagni C. The FMRP regulon: From targets to disease convergence. Front Neurosci. 2013; 7:191.

5. 5. Tassone F, Iong KP, Tong T-H, Lo J, Gane LW, Berry-Kravis E, Nguyen D, Mu LY, Laffin J, Bailey DB, Hagerman RJ. FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States. Genome Med. 2012; 4:100.

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