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About this Biochemistry, Genetics and Molecular Biology article
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 by Lusk, Laina (author);Black, Emily (author);Vengoechea, Jaime (author) is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Lusk, Laina (author);Black, Emily (author);Vengoechea, Jaime (author)
- Publisher
- BMJ Publishing Group
- Published
- 2019
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)
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