S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mou...
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse
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Author / Creator
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publisher
London: Nature Publishing Group UK
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Contents
Progressive hearing loss is very common in the population but we still know little about the underlying pathology. A new spontaneous mouse mutation (stonedeaf,
stdf
) leading to recessive, early-onset progressive hearing loss was detected and exome sequencing revealed a Thr289Arg substitution in Sphingosine-1-Phosphate Receptor-2 (
S1pr2<...
Alternative Titles
Full title
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4935955
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4935955
Other Identifiers
ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/srep28964
