DFNB10
DFNB10
Abbreviation for:
deafness autosomal recessive type 10Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
References in periodicals archive
In the Dutch family, the c.323-6G>A mutation was (relatively) severe and homozygous mutation results in prelingual (DFNB10) hearing impairment.
Compound heterozygosity for a mild and severe mutation leads to postlingual hearing loss (DFNB8), whereas the combination of two severe mutations leads to profound hearing impairment with prelingual onset (DFNB10) [4].
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