Loss of FAM111B protease mutated in hereditary fibrosing poikiloderma negatively regulates telomere length
<p>Hereditary fibrosing poikiloderma (HFP) is a rare human dominant negative disorder caused by mutations in the <em>FAM111B</em> gene that encodes a nuclear trypsin-like serine protease. HFP patients present with symptoms including skin abnormalities, tendon cont...
| Main Authors: | , , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
Frontiers Media
2023
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