Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3. (Q34576838)

3 August 2017

title

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3. (English)

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autosomal recessive nonsyndromic deafness

3 August 2017

main subject

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10

Thomas B Friedman

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2

Saima Riazuddin

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11

Sheikh Riazuddin

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4

Saima Anwar

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7

Shaheen N Khan

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8

Tayyab Husnain

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6

S Amer Riazuddin

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Shahid Y Khan

1

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Muhammad Tariq

series ordinal

3

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Muhammad I Shabbir

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5

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Zubair M Ahmed

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9

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publication date

26 October 2006

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3 August 2017

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volume

120

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issue

6

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page(s)

789-793

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KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

3 August 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS00439-006-0275-1

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

21 January 2018

1 reference

12 December 2020

Expression pattern of the FGF-related proto-oncogene int-2 suggests multiple roles in fetal development.

1 reference

12 December 2020

Faster linkage analysis computations for pedigrees with loops or unused alleles.

1 reference

12 December 2020

Comprehensive genome and transcriptome analysis of the 11q13 amplicon in human oral cancer and synteny to the 7F5 amplicon in murine oral carcinoma

1 reference

12 December 2020

DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter.

1 reference

12 December 2020

Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

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12 December 2020

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

1 reference

12 December 2020

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

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12 December 2020

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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12 December 2020

A simple and efficient non-organic procedure for the isolation of genomic DNA from blood

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Shank2 associates with and regulates Na+/H+ exchanger 3

1 reference

12 December 2020

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

12 December 2020

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

1 reference

12 December 2020

Human Nonsyndromic Sensorineural Deafness

1 reference

12 December 2020

A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.

1 reference

12 December 2020

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

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12 December 2020

Non-syndromic, autosomal-recessive deafness

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12 December 2020

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

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12 December 2020

Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear

1 reference

12 December 2020

Newborn hearing screening--a silent revolution

1 reference

12 December 2020

10.1007/S00439-006-0275-1

Identifiers

DOI

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Dimensions Publication ID

3 August 2017

1012481877

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