Skip to search formSkip to main contentSkip to account menu

DEAFNESS, AUTOSOMAL RECESSIVE 15

Known as: DFNB72, DEAFNESS, AUTOSOMAL RECESSIVE 95, DFNB15 
National Institutes of Health

Related topics

Related topics

3 relations
Autosomal recessive inheritanceGIPC3 gene

Broader (1)

Sensorineural Hearing Loss (disorder)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family
With homozygosity mapping we have identified two large homozygous regions on chromosome 3q13.11–q13.31 and chromosome 19p13.3–q31… 
2008
2008
[A new locus for an autosomal dominant, non-syndromic hearing impairment (DFNA57) located on chromosome 19p13.2 and overlapping with DFNB15].
BACKGROUND Non-syndromic hearing loss is the most genetically heterogeneous trait known in humans. To date, 54 loci for autosomal… 
2008
2008
Ein neuer Genort für eine autosomal dominante, nichtsyndromale Hörstörung (DFNA57) kartiert auf Chromosom 19p13.2 und überlappt mit DFNB15
ZusammenfassungHintergrundDer nichtsyndromale Hörverlust ist die Erkrankung, für die beim Menschen bislang die häufigsten… 
2001
2001
MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.
BACKGROUND Earlier studies have mapped the autosomal recessive nonsyndromic deafness locus, DFNB15, to chromosomes 3q21.3-q25.2… 
2001
2001
MYO 1 F as a Candidate Gene for Nonsyndromic Deafness , DFNB 15
  • 2001
  • Corpus ID: 37754562
Background: Earlier studies have mapped the autosomal recessive nonsyndromic deafness locus, DFNB15, to chromosomes 3q21.3-q25.2… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)