A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress
Mutations in the gene AK2 are responsible for reticular dysgenesis (RD), a rare and severe form of primary immunodeficiency in children. RD patients have a severely shortened life expectancy and without treatment die, generally from sepsis soon after birth. The only available therapeutic option for...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
| Published: |
The Company of Biologists,
2019-12-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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