Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant is a research paper published in Molecular Genetics & Genomic Medicine (2022). On theSindex it has a DataRank of 0. It has been cited 3 times.
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NIDCD NIH HHS
Grant: R01 DC003594
NIDCD NIH HHS
Grant: R01 DC011651
National Institutes of Health
Grant: 5R01DC003594-13
Identification of Autosomal Recessive Nonsyndromic Hearing Impairment Genes
National Institutes of Health
Grant: 5R01DC011651-02
Localization of nonsyndromic hearing impairment genes
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