Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms-Reference-Cited by-同舟云学术

Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms

Published:2005-04 Issue:3 Volume:27 Page:211-217
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Fukuda Takayuki,Yamashita Yushiro,Nagamitsu Shinichiro,Miyamoto Kenichi,Jin Jing-Ji,Ohmori Iori,Ohtsuka Yoko,Kuwajima Katsuko,Endo Shoichi,Iwai Tsuyako,Yamagata Hidehisa,Tabara Yasuharu,Miki Tetsuro,Matsuishi Toyojiro,Kondo Ikuko

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference41 articles.

1. A progressive synfrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases;Hagberg;Ann Neurol,1983

2. Rett syndrome: history and general overview;Rett;Am J Med Genet,1986

3. Diagnostic criteria for rett syndrome

4. Rett variants: a suggested model for inclusion criteria;Hagberg;Pediatr Neurol,1994

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

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