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Rett syndrome and MeCP2: linking epigenetics and neuronal function.

作者信息

Shahbazian Mona D, Zoghbi Huda Y

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Am J Hum Genet. 2002 Dec;71(6):1259-72. doi: 10.1086/345360. Epub 2002 Nov 19.

Abstract
摘要

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本文引用的文献

1
Balanced X chromosome inactivation patterns in the Rett syndrome brain.
Am J Med Genet. 2002 Aug 1;111(2):164-8. doi: 10.1002/ajmg.10557.
4
Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome.
J Child Neurol. 2002 Jan;17(1):33-6. doi: 10.1177/088307380201700108.
5
Rett syndrome: clinical manifestations in males with MECP2 mutations.
J Child Neurol. 2002 Jan;17(1):20-4. doi: 10.1177/088307380201700105.
6
Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.
Eur J Hum Genet. 2002 Jan;10(1):77-81. doi: 10.1038/sj.ejhg.5200745.
7
A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome.
Am J Hum Genet. 2002 Apr;70(4):1034-7. doi: 10.1086/339553. Epub 2002 Feb 15.
9
Methylation-dependent silencing at the H19 imprinting control region by MeCP2.
Nucleic Acids Res. 2002 Mar 1;30(5):1139-44. doi: 10.1093/nar/30.5.1139.

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