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Deafness, Autosomal Recessive 22
Known as:
DFNB22
National Institutes of Health
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Related topics
Related topics
3 relations
Autosomal recessive inheritance
OTOA, GLY451ASP
Broader (1)
Sensorineural Hearing Loss (disorder)
Papers overview
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2010
2010
Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families
R. Badr
,
Bahareh Shoja-Saffar
,
Niloofar Bazzaz-Zadegan
,
K. Jalalvand
,
K. Kahrizi
,
H. Najmabadi
2010
Corpus ID: 74347238
Objective: Hearing impairment is the most frequent sensorineural defect in 2 forms, syndromic and non–syndromic. The aim of this…
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