Compound heterozygosity at two different loci in hereditary hearing loss. (a) Autosomal recessive hearing loss due to mutations in the gene connexin 26.

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Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
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Compound heterozygosity at two different loci in hereditary hearing loss. (a) Autosomal recessive hearing loss due to mutations in the gene connexin 26. (b) Autosomal recessive hearing loss due to deletions in the gene connexin 30. (c) Compound heterozygosity for a connexin 26 mutation and a connexin 30 deletion also produces hearing loss. This could be termed "digenic" inheritance. Source: Atypical Modes of Inheritance, Medical Genetics: An Integrated Approach Citation: Schaefer G, Thompson, Jr. JN. Medical Genetics: An Integrated Approach; 2017 Available at: https://accessmedicine.mhmedical.com/DownloadImage.aspx?image=/data/books/2247/schaefer_ch12_f013-1.png&sec=173745108&BookID=2247&ChapterSecID=173745036&imagename= Accessed: January 07, 2018 Copyright © 2018 McGraw-Hill Education. All rights reserved

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