A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration...
A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress
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Publisher
England: The Company of Biologists Ltd
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Language
English
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England: The Company of Biologists Ltd
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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 early after birth. The only available therapeutic option for RD is hematopoietic stem cell transplantation (HS...
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A model for reticular dysgenesis shows impaired sensory organ development and hair cell regeneration linked to cellular stress
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TN_cdi_doaj_primary_oai_doaj_org_article_e8c09681320d4b5b98b218bcea9563f8
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e8c09681320d4b5b98b218bcea9563f8
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ISSN
1754-8403
E-ISSN
1754-8411
DOI
10.1242/dmm.040170