A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family
Abstract Background To investigate the clinical features and the underlying causal gene of a family with hereditary late-onset deafness in Inner Mongolia of China, and to provide evidence for the early genetic screening and diagnosis of this disease. Methods Family data were collected to draw a pedi...
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Main Authors: | , , , , , , , , |
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Format: | Book |
Published: |
BMC,
2019-03-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |