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PDFPhenotypes
Short report
Segregation of two variants suggests the presence of autosomal dominant and recessive forms of WFS1-related disease within the same family: expanding the phenotypic spectrum of Wolfram Syndrome
- Correspondence to Dr Jaime Vengoechea, Human Genetics, Emory University, Atlanta, GA 30322, USA; jvengoe{at}emory.edu
Citation
Segregation of two variants suggests the presence of autosomal dominant and recessive forms of WFS1-related disease within the same family: expanding the phenotypic spectrum of Wolfram Syndrome
Publication history
- Received October 3, 2018
- Revised May 29, 2019
- Accepted June 22, 2019
- First published July 30, 2019.
Online issue publication
January 23, 2020
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© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.