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A Novel Frameshift Mutation of the USH2A Gene in a Korean Patient with Usher Syndrome Type II
Sung Hyun Boo, Min-Jung Song, Hee-Jin Kim, Yang-Sun Cho, Hosuk Chu, Moon-Hee Ko, Won-Ho Chung, Jong-Won Kim, Sung Hwa Hong
Clinical and Experimental Otorhinolaryngology. 2013;6(1):41-44.   Published online 2011 October 1    DOI: https://doi.org/10.3342/ceo.2013.6.1.41

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A Novel Frameshift Mutation of theUSH2AGene in a Korean Patient with Usher Syndrome Type II
Clinical and Experimental Otorhinolaryngology. 2013;6(1):41   Crossref logo
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Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II
Human Mutation. 2008;29(3):451-451   Crossref logo
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Targeted Exome Sequencing Identified a Novel USH2A Mutation in a Chinese Usher Syndrome Family
. 2020;   Crossref logo
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Whole exome sequencing identifies a novel frameshift mutation in GPC3 gene in a patient with overgrowth syndrome
Gene. 2015;572(2):303-306   Crossref logo
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Targeted exome sequencing identified a novel USH2A mutation in a Chinese Usher syndrome family: a case report
. 2020;   Crossref logo
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Targeted exome sequencing identified a novel USH2A mutation in a Chinese Usher syndrome family: a case report
. 2020;   Crossref logo
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Identification of 51 Novel Exons of the Usher Syndrome Type 2A (USH2A) Gene That Encode Multiple Conserved Functional Domains and That Are Mutated in Patients with Usher Syndrome Type II
The American Journal of Human Genetics. 2004;74(4):738-744   Crossref logo
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Targeted exome sequencing identified a novel USH2A mutation in a Chinese Usher syndrome family: a case report
. 2020;   Crossref logo
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Targeted exome sequencing identified a novel USH2A mutation in a Chinese Usher syndrome family: a case report
. 2020;   Crossref logo
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Targeted exome sequencing identified a novel USH2A mutation in a Chinese Usher syndrome family: a case report
. 2020;   Crossref logo
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