Apolipoprotein E genotype analysis in Chinese Han ethnic children with Wilson's disease, with a concentration on those homozygous for R778L
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
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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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1. A Systematic Review and Meta-Analysis of the R778L Mutation in ATP7B With Wilson Disease in China;Pediatric Neurology;2023-08
2. Wilson’s Disease—Genetic Puzzles with Diagnostic Implications;Diagnostics;2023-03-29
3. Management Perspective of Wilson’s Disease: Early Diagnosis and Individualized Therapy;Current Neuropharmacology;2021-04-07
4. Difference in iron metabolism may partly explain sex-related variability in the manifestation of Wilson’s disease;Journal of Trace Elements in Medicine and Biology;2020-12
5. Effect of homeostatic iron regulator protein gene mutation on Wilson's disease clinical manifestation: original data and literature review;International Journal of Neuroscience;2020-11-18
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