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Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome
by
Riahi, Zied
,
Zainine, Rim
,
Mellouli, Yosra
,
Hannachi, Raja
,
Bouyacoub, Yosra
,
Laroussi, Nadia
,
Beltaief, Najeh
,
Kefi, Rym
,
Romdhane, Lilia
,
Bonnet, Crystel
,
Abdelhak, Sonia
,
Besbes, Ghazi
Published in
International journal of pediatric otorhinolaryngology
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International Journal Of Pediatric Otorhinolaryngology
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Subjects
Audiometry
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Child, Preschool
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Cochlear Implant
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Cochlear Implantation - Methods
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Cochlear Implants
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Connexin 26
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Connexins - Genetics
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Deafness - Genetics
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Deafness - Surgery
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Dominant
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Female
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Follow-Up Studies
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Genetic Carrier Screening - Methods
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Genetic Predisposition To Disease
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Genetic Testing
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Gjb2
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Hearing Loss
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Hearing Loss, Sensorineural - Diagnosis
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Hearing Loss, Sensorineural - Genetics
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Hearing Loss, Sensorineural - Surgery
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