Distribution of AGG interruption patterns within nine world populations-Reference-Cited by-同舟云学术

Distribution of AGG interruption patterns within nine world populations

Published:2014 Issue:4 Volume:3 Page:153-161
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Yrigollen Carolyn M.¹,Sweha Stefan¹,Durbin-Johnson Blythe²,Zhou Lili³,Berry-Kravis Elizabeth³,Fernandez-Carvajal Isabel⁴,Faradz Sultana MH⁵,Amiri Khaled⁶,Shaheen Huda⁶,Polli Roberta⁷,Murillo-Bonilla Luis⁸,de Jesus Silva Arevalo Gabriel⁹,Cogram Patricia¹⁰,Murgia Alessandra⁷,Tassone Flora¹¹¹

Affiliation:

1. Department of Biochemistry and Molecular Medicine, University of California Davis, School of Medicine

2. Department of Public Health Sciences, University of California Davis, School of Medicine

3. Department of Pediatrics, Neurological Sciences, Biochemistry, Rush University Medical Center

4. Laboratorio de Enfermedades genéticas y cribado neonatal, Departamento de Genetica Molecular de la Enfermedad, Instituto de Biologìa y Genética Molecular Universidad de Valladolid-CSIC

5. Center for Biomedical Research, Diponegoro University

6. Department of Biology, College of Science, United Arab University

7. Laboratory of Molecular Genetics of Neurodevelopment, Department of Women’s and Children’s Health, University of Padova

8. Autonomous University of Guadalajara, Faculty of Medicine

9. Genetic and Neurometabolic Clinic, Obras Sociales Santo Hermano Pedro, Antigua Guatemala. Center by BiomedicalResearch, Medicine school San Carlos University

10. Biomedicine Division, Fraunhofer Chile Research Foundation

11. I.N.D. Institute, University of California Davis Medical Center

Publisher

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

Subject

General Medicine

Reference47 articles.

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2. 2. Hagerman R, Hagerman P. Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. Lancet Neurol. 2013; 12:786-798.

3. 3. Fu YH, Kuhl DP, Pizzuti A, et al. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox. Cell. 1991; 67:1047-1058.

4. 4. McMurray CT. Mechanisms of trinucleotide repeat instability during human development. Nat Rev Genet. 2010; 11:786-799.

5. 5. Eichler EE, Hammond HA, Macpherson JN, Ward PA, Nelson DL. Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions. Hum Mol Genet. 1995; 4:2199-2208.

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