标题
Variants of human
CLDN9
cause mild to profound hearing loss
作者
关键词
-
出版物
HUMAN MUTATION
Volume 42, Issue 10, Pages 1321-1335
出版商
Wiley
发表日期
2021-07-16
DOI
10.1002/humu.24260
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies
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- (2012) Zil-e-Huma Bashir et al. JOURNAL OF HUMAN GENETICS
- HHblits: lightning-fast iterative protein sequence searching by HMM-HMM alignment
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- Mutations in CLDN14 are associated with different hearing thresholds
- (2010) Rasheeda Bashir et al. JOURNAL OF HUMAN GENETICS
- Statistical potentials for fold assessment
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- Fast and accurate automatic structure prediction with HHpred
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- A Claudin-9–Based Ion Permeability Barrier Is Essential for Hearing
- (2009) Yoko Nakano et al. PLoS Genetics
- Formation of tight junction: determinants of homophilic interaction between classic claudins
- (2007) Jörg Piontek et al. FASEB JOURNAL
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