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A Novel Splicing Mutation in COL11A1 as a Cause of Dominant Progressive Nonsyndromic Hearing Loss.


NE-Munroe-Meyer Institute of Genetics & Rehabilitation, UCEDD/LEND
Program TypeUCEDD Fiscal Year 2016
Date of Publication02/2015 Author(s)Shelley Smith
Type of Material
A Novel Splicing Mutation in COL11A1 as a Cause of Dominant Progressive Nonsyndromic Hearing Loss.
Annual Midwinter Meeting of the Association for Research in Otolaryngology, Baltimore, MD, Feb. 24.
Publisher 0
Brief Description
Target Audience
Ordering Information
Name Shelley Smith, Ph.D.
Address
Phone 402-559-5314    
Email [email protected]
To Obtain Copies (URL or Email) [email protected]