Apolipoprotein E genotype analysis in Chinese Han ethnic children with Wilson's disease, with a concentration on those homozygous for R778L

Author:

Gu Yan-Hong,Kodama Hiroko,Du Si-Lian

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference16 articles.

1. Toxicology of metals;Kodama,1996

2. A nation-wide survey for neurologic and hepato-neurologic type of Wilson disease: clinical features and hepatic copper content (in Japanese);Shimizu;No To Hattatsu (Tokyo),1996

3. Mutation spectrum and polymorphisms in ATP7B identified on direct sequencing of all exons in Chinese Han and Hui ethnic patients with Wilson's disease;Gu;Clin Genet,2003

4. Haplotype and mutation analysis in Japanese patients with Wilson disease;Nanji;Am J Hum Genet,1997

5. Identification of novel mutations and the three most common mutations in the human ATP7B gene of Korean patients with Wilson disease;Yoo;Genet Med,2002

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