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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Bibliographic Details
Main Authors: Alberto Rissone (Author), Erin Jimenez (Author), Kevin Bishop (Author), Blake Carrington (Author), Claire Slevin (Author), Stephen M. Wincovitch (Author), Raman Sood (Author), Fabio Candotti (Author), Shawn M. Burgess (Author)
Format: Book
Published: The Company of Biologists, 2019-12-01T00:00:00Z.
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3rd Floor Main Library

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