Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome-Reference-Cited by-同舟云学术

Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome

Published:2016-11-09 Issue:11 Volume:11 Page:e0165550
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Ward Christopher S.,Huang Teng-Wei,Herrera José A.,Samaco Rodney C.,Pitcher Meagan R.,Herron Alan,Skinner Steven A.,Kaufmann Walter E.,Glaze Daniel G.,Percy Alan K.,Neul Jeffrey L.

Funder

National Institute of Child Health and Human Development

NIH Office of the Director

National Institute of Neurological Disorders and Stroke

International Rett Syndrome Foundation

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference49 articles.

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3. Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome;JL Neul;Neurology,2008

4. Rett syndrome: revised diagnostic criteria and nomenclature;JL Neul;Annals of neurology,2010

5. Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome;MD McCauley;Science translational medicine,2011

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