Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling.Timing of cochlear implantation in auditory neuropathy patients with OTOF mutations: Our experience with 10 patients.

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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2015 nî lūn-bûn

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2015 թուականին հրատարակուած գիտական յօդուած

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2015 թվականին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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prefLabel

Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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P1476

Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

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P2093

Che-Ming Wu

http://www.w3.org/2001/XMLSchema#string

Chen-Chi Wu

http://www.w3.org/2001/XMLSchema#string

Chin-Kuo Chen

http://www.w3.org/2001/XMLSchema#string

Hui-Chen Ko

http://www.w3.org/2001/XMLSchema#string

Ju-Li Lin

http://www.w3.org/2001/XMLSchema#string

Pei-Lung Chen

http://www.w3.org/2001/XMLSchema#string

Yin-Hung Lin

http://www.w3.org/2001/XMLSchema#string

P2860

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

A mutation in PDS causes non-syndromic recessive deafness

Timing of surgical intervention with cochlear implant in patients with large vestibular aqueduct syndrome

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing.

Advancing genetic testing for deafness with genomic technology.

Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS.

Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis

Spoken language development in children following cochlear implantation.

Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics?

Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment

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e0138575

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scholarly article

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10.1371/JOURNAL.PONE.0138575

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English

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Yung-Ting Tsou

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2015-01-01T00:00:00Z

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282126147

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Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

about

P2860

P2860

Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P932