SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

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Mouse models for pendrin-associated loss of cochlear and vestibular function Functional Testing of SLC26A4 Variants-Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria.

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SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

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2013 nî lūn-bûn

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SLC26A4 mutation testing for h ...... nt of the vestibular aqueduct.

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SLC26A4 mutation testing for h ...... nt of the vestibular aqueduct.

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SLC26A4 mutation testing for h ...... nt of the vestibular aqueduct.

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SLC26A4 mutation testing for h ...... nt of the vestibular aqueduct.

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SLC26A4 mutation testing for h ...... nt of the vestibular aqueduct.

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SLC26A4 mutation testing for h ...... nt of the vestibular aqueduct.

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P2093

Andrew J Griffith

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Byung Yoon Choi

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Carmen C Brewer

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

Christopher K Zalewski

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Julie Muskett

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

Kelly A King

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Kyu Yup Lee

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Parna Chattaraj

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Philine Wangemann

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

Seth L Alper

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P2860

The Pendred syndrome gene encodes a chloride-iodide transport protein

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

Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending

Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

Molecular analysis of the PDS gene in Pendred syndrome

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice

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scholarly article

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10.5319/WJO.V3.I2.26

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257922765

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25960948

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4423814

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SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

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P2860

P2860

SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

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