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Title
Exome Sequencing Identifies ZNF644 Mutations in High Myopia
Authors
Keywords
Myopia, Eyes, Gene sequencing, Han Chinese people, Genomic databases, Mutation, Genome sequencing, Mutation databases
Journal
PLoS Genetics
Volume 7, Issue 6, Pages e1002084
Publisher
Public Library of Science (PLoS)
Online
2011-06-18
DOI
10.1371/journal.pgen.1002084
References
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- Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82
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- TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing
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- X-linked myopia: Bornholm Eye Disease
- (2010) Marianne Schwartz et al. CLINICAL GENETICS
- Exome sequencing: the sweet spot before whole genomes
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- Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
- (2010) Kaya Bilgüvar et al. NATURE
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- Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing
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- Exome sequencing identifies the cause of a mendelian disorder
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- (2009) Murim Choi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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- Prevalence of Myopia in Urban and Rural Children in Mainland China
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- Identification and Replication of Three Novel Myopia Common Susceptibility Gene Loci on Chromosome 3q26 using Linkage and Linkage Disequilibrium Mapping
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