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Deafness, Autosomal Recessive 9
Known as:
DFNB9
, NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 9
, AUDITORY NEUROPATHY, AUTOSOMAL RECESSIVE, 1
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National Institutes of Health
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Related topics
Related topics
2 relations
Autosomal recessive inheritance
Sensorineural Hearing Loss (disorder)
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
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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2006
2006
Estudio genético-molecular de las hipoacusias no sindrómicas de tipos DFNB1 y DFNB9
M. Ballesteros
2006
Corpus ID: 163571838
La hipoacusia de tipo DFNB1, causada por mutaciones en el gen de la conexina 26 (GJB2) en 13q12, es el subtipo mas frecuente de…
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2006
2006
Physiopathologie de la surdité DFNB9 : identification de l'otoferline comme composant essentiel de l'exocytose des synapses à ruban des cellules sensorielles auditives
I. Roux
2006
Corpus ID: 82723162
Plusieurs mutations du geneOTOF ont ete identifiees comme responsables de la surdite autosomique recessive DFNB9. Ce gene code…
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