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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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TheScientificWorldJOURNAL
2001
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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. |
format | Online Article Text |
id | pubmed-6083949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | TheScientificWorldJOURNAL |
record_format | MEDLINE/PubMed |
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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