Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A. (Q50356353)

6 March 2018

title

Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A. (English)

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6 March 2018

author

Heidi L. Rehm

2

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6 March 2018

Bassam R. Ali

6

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6 March 2018

Lihadh Al-Gazali

7

object named as

Lihadh Al-Gazali

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6 March 2018

Salma Ben-Salem

1

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6 March 2018

Patrick J Willems

3

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6 March 2018

Zakaria A Tamimi

4

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6 March 2018

Hammadi Ayadi

5

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6 March 2018

publication date

6 November 2013

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6 March 2018

Molecular Biology Reports

published in

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6 March 2018

volume

41

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6 March 2018

issue

1

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6 March 2018

page(s)

193-200

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6 March 2018

Non-syndromic, autosomal-recessive deafness

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

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Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.

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A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family

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Identifiers

DOI

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6 March 2018

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6 March 2018