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Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner

Inheritance of a deafness-causing genotype does not necessarily mean that a person will have profound hearing loss. The presence of a modifying gene can change the effect of the deafness genotype. As an example, mutations found commonly among the deaf are at times found among their normal hearing re...

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Detalles Bibliográficos
Autores principales: Wilcox, Edward, Riazuddin, Saima, Riazuddin, Sheikh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083949/
https://www.ncbi.nlm.nih.gov/pubmed/12805671
http://dx.doi.org/10.1100/tsw.2001.40
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author Wilcox, Edward
Riazuddin, Saima
Riazuddin, Sheikh
author_facet Wilcox, Edward
Riazuddin, Saima
Riazuddin, Sheikh
author_sort Wilcox, Edward
collection PubMed
description Inheritance of a deafness-causing genotype does not necessarily mean that a person will have profound hearing loss. The presence of a modifying gene can change the effect of the deafness genotype. As an example, mutations found commonly among the deaf are at times found among their normal hearing relatives [1]. The implication is that there are genes or gene products whose interactions allow the normal physiological function of the inner ear despite a mutation that would normally disrupt the process. Deafness is not the first disorder in which modifiers can change the expected outcome, nor will it be the last, but it is very unusual for the outcome to be so dramatically changed.
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spelling pubmed-60839492018-08-26 Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner Wilcox, Edward Riazuddin, Saima Riazuddin, Sheikh ScientificWorldJournal Directions in Science Inheritance of a deafness-causing genotype does not necessarily mean that a person will have profound hearing loss. The presence of a modifying gene can change the effect of the deafness genotype. As an example, mutations found commonly among the deaf are at times found among their normal hearing relatives [1]. The implication is that there are genes or gene products whose interactions allow the normal physiological function of the inner ear despite a mutation that would normally disrupt the process. Deafness is not the first disorder in which modifiers can change the expected outcome, nor will it be the last, but it is very unusual for the outcome to be so dramatically changed. TheScientificWorldJOURNAL 2001-05-01 /pmc/articles/PMC6083949/ /pubmed/12805671 http://dx.doi.org/10.1100/tsw.2001.40 Text en Copyright © 2001 Edward Wilcox et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Directions in Science
Wilcox, Edward
Riazuddin, Saima
Riazuddin, Sheikh
Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner
title Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner
title_full Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner
title_fullStr Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner
title_full_unstemmed Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner
title_short Some Deafness-Causing Mutations Can Be Silenced with the Appropriate Gene Partner
title_sort some deafness-causing mutations can be silenced with the appropriate gene partner
topic Directions in Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083949/
https://www.ncbi.nlm.nih.gov/pubmed/12805671
http://dx.doi.org/10.1100/tsw.2001.40
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