RGD Annotation Report for Sudden Hearing LossRat Genome Database

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An association has been curated linking NOS3 and Sudden Hearing Loss in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from Teranishi M, etal., Free Radic Res. 2013 Jul;47(6-7):498-506. doi: 10.3109/10715762.2013.793319. Epub 2013 May 7.
2 additional annotations were made from Teranishi M, etal., Free Radic Res. 2013 Jul;47(6-7):498-506. doi: 10.3109/10715762.2013.793319. Epub 2013 May 7.
17 RGD objects have been annotated to Sudden Hearing Loss (DOID:9003817)
240 papers in RGD have been used to annotate NOS3
Curation Notes: DNA:snp:cds:p.E298D (rs1799983) (human)

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.