How to cite this article: Francey LJ, Conlin LK, Kadesch HE, Clark D, Berrodin D, Sun Y, Glessner J, Hakonarson H, Jalas C, Landau C, Spinner NB, Kenna M, Sagi M, Rehm HL, Krantz ID. 2012. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Am J Med Genet Part A 158A:298–308.
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment†
Article first published online: 6 DEC 2011
Copyright © 2011 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 2, pages 298–308, February 2012
How to Cite
Francey, L. J., Conlin, L. K., Kadesch, H. E., Clark, D., Berrodin, D., Sun, Y., Glessner, J., Hakonarson, H., Jalas, C., Landau, C., Spinner, N. B., Kenna, M., Sagi, M., Rehm, H. L. and Krantz, I. D. (2012), Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Am. J. Med. Genet., 158A: 298–308. doi: 10.1002/ajmg.a.34391
- Issue published online: 19 JAN 2012
- Article first published online: 6 DEC 2011
- Manuscript Accepted: 14 OCT 2011
- Manuscript Received: 16 FEB 2011
- NIDCD (IDK). Grant Numbers: R33DC008630, R33DC008630-03S1
- CHOP Institutional Development Funds (IDK)
Additional supporting information may be found in the online version of this article.
|ajmg_34391_sm_SupplTab2.doc||54K||Table II: Summary of all Missense Variants and Deletions Found by Sanger Sequencing|
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