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Publications by Sanaz Arzhanginy
Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss
Laryngoscope
Otorhinolaryngology
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Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population
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Variants Encoding a Restricted Carboxy-Terminal Domain of SLC12A2 Cause Hereditary Hearing Loss in Humans
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Myo1c Mutations Associated With Hearing Loss Cause Defects in the Interaction With Nucleotide and Actin
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Congenital Cytomegalovirus Infection: A Cause of Sensorineural Hearing Loss.
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Mutations in Mitochondrial Histidyl tRNA Synthetase HARS2 Cause Ovarian Dysgenesis and Sensorineural Hearing Loss of Perrault Syndrome
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Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population
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Novel PTPRQ Mutations Identified in Three Congenital Hearing Loss Patients With Various Types of Hearing Loss
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SMARCB1 Mutations Are Not a Common Cause of Multiple Meningiomas
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Labyrinthine Window Rupture as a Cause of Acute Sensorineural Hearing Loss
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