Variants of human CLDN9 cause mild to profound hearing loss is a research paper published in Human Mutation (2021). On theSindex it has a DataRank of 0. It has been cited 6 times.
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Higher Education Commission, Pakistan
Grant: 3288
NIDCD NIH HHS
Grant: T32 DC000039
Intramural NIH HHS
Grant: Z01 DC000048
Intramural NIH HHS
Grant: Z01 DC000039
NIDCD NIH HHS
Grant: R01 DC014953
National Institute on Deafness and Other Communication Disorders
FWCI
0.43
Citation Percentile
0.6%
Citation Trend
Fields of Study
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Sustainable Development Goals