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DEAFNESS, AUTOSOMAL RECESSIVE 89
Known as:
DFNB89
National Institutes of Health
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2 relations
Autosomal recessive inheritance
KARS, TYR173HIS
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2011
2011
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2
S. Basit
,
Kwanghyuk Lee
,
+8 authors
S. Leal
Human Genetics
2011
Corpus ID: 9731086
DFNB89 is a novel autosomal recessive nonsyndromic hearing impairment (ARNSHI) locus that was mapped to 16q21-q23.2. Linkage to…
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