Deleterious mutation in GPSM2 identified as cause for nonsyndromic deafness

Affiliations

Comment

Jm Schulze. Clin Genet. 2011 Jan.

. 2011 Jan;79(1):44-5.

doi: 10.1111/j.1399-0004.2010.01556_1.x. Epub 2010 Oct 12.

¹ Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, 950 West 28th Avenue, Vancouver, BC, Canada. jschulze@cmmt.ubc.ca

No abstract available

Comment on

Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.
Walsh T, Shahin H, Elkan-Miller T, Lee MK, Thornton AM, Roeb W, Abu Rayyan A, Loulus S, Avraham KB, King MC, Kanaan M. Walsh T, et al. Am J Hum Genet. 2010 Jul 9;87(1):90-4. doi: 10.1016/j.ajhg.2010.05.010. Epub 2010 Jun 17. Am J Hum Genet. 2010. PMID: 20602914 Free PMC article.