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Reference Patent

Reference - List

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  • Search Condition : Filter (MeSH = Deafness / genetics)
Species Resource RRC ID Title Journal Published Link
Human and Animal Cells 293T(RCB2202) 58863 Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans. PLoS Genet 2020-4-1 Pubmed Full text
C.elegans tm1175 , tm10457 56175 CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease. Physiol Rev 2018-7-1 Pubmed Full text
Human and Animal Cells HMV-II(RCB0777) 42737 Functional difference of the SOX10 mutant proteins responsible for the phenotypic variability in auditory-pigmentary disorders. J Biochem 2006-10-1 Pubmed Full text
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