1. Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations. Issue 9 (19th July 2013) Authors: Gallant, Emily; Francey, Lauren; Tsai, Ellen A.; Berman, Micah; Zhao, Yaru; Fetting, Heather; Kaur, Maninder; Deardorff, Matthew A.; Wilkens, Alisha; Clark, Dinah; Hakonarson, Hakon; Rehm, Heidi L.; Krantz, Ian D. Journal: American journal of medical genetics Issue: Volume 161:Issue 9(2013:Sep.) Page Start: 2148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations. Issue 9 (19th July 2013) Authors: Gallant, Emily; Francey, Lauren; Tsai, Ellen A.; Berman, Micah; Zhao, Yaru; Fetting, Heather; Kaur, Maninder; Deardorff, Matthew A.; Wilkens, Alisha; Clark, Dinah; Hakonarson, Hakon; Rehm, Heidi L.; Krantz, Ian D. Journal: American journal of medical genetics Issue: Volume 161:Issue 9(2013:Sep.) Page Start: 2148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗