Familial cases and male cases with MECP2 mutations-Reference-Cited by-同舟云学术

Familial cases and male cases with MECP2 mutations

Published:2017-04-10 Issue:4 Volume:174 Page:451-457
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zhang Qingping¹^ORCID,Zhao Ying¹,Bao Xinhua¹,Luo Jinjun²,Zhang Xiaoying¹,Li Jiarui³,Wei Liping³,Wu Xiru¹

Affiliation:

1. Department of Pediatrics; Peking University First Hospital; Beijing China

2. Departments of Neurology and Pharmacology; Lewis Katz School of Medicine at Temple University; Philadelphia Pennsylvania

3. State Key Laboratory of Protein and Plant Gene Research; School of Life Sciences; Peking University, Center for Bioinformatics; Beijing China

Funder

Peking University

Clinical Hospital Cooperation Project

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference39 articles.

1. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;American Journal of Human Genetics,1992

2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nature Genetics,1999

3. Variable phenotypic expression of a MECP2 mutation in a family;Augenstein;Journal of Neurodevelopmental Disorders,2009

4. Methylation-dependent and -independent genomic targeting principles of the MBD protein family;Baubec;Cell,2013

5. Investigating genotype-phenotype relationships in Rett syndrome using an international data set;Bebbington;Neurology,2008

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