Asplenia
Author:
Publisher
Elsevier
Reference41 articles.
1. Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module;Koss;Dev Cell,2012
2. Ivemark’s “asplenia” syndrome: a single gene disorder;McChane;South Med J,1989
3. Rice. Infections of people with complement deficiencies and patients who have undergone splenectomy;Sanjay;Clin Microbiol Rev,2010
4. Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others;Gilbert;Eur J Pediatr,2002
5. Development and function of the mammalian spleen;Brendolan;Bioessays,2007
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1. Asplenia and spleen hypofunction;Nature Reviews Disease Primers;2022-11-03
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