Novel MSX1 variants identified in families with nonsyndromic oligodontia
Abstract The goal of this study was to identify MSX1 gene variants in multiple Chinese families with nonsyndromic oligodontia and analyse the functional influence of these variants. Whole-exome sequencing (WES) and Sanger sequencing were performed to identify the causal gene variants in five familie...
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मुख्य लेखकों: | , , , , , , |
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स्वरूप: | पुस्तक |
प्रकाशित: |
Nature Publishing Group,
2021-01-01T00:00:00Z.
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ऑनलाइन पहुंच: | Connect to this object online. |
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बोधानक: |
A1234.567 |
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प्रति 1 | उपलब्ध |