Extending the Clinical Phenotype of Adenosine Deaminase 2 Deficiency-Reference-Cited by-同舟云学术

Extending the Clinical Phenotype of Adenosine Deaminase 2 Deficiency

Published:2016-10 Issue: Volume:177 Page:316-320
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Ben-Ami Tal,Revel-Vilk Shoshana,Brooks Rebecca,Shaag Avraham,Hershfield Michael S.,Kelly Susan J.,Ganson Nancy J.,Kfir-Erenfeld Shlomit,Weintraub Michael,Elpeleg Orly,Berkun Yackov,Stepensky Polina

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference25 articles.

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4. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD);Chakraborty;Blood,2014

5. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy;Navon Elkan;N Engl J Med,2014

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3. Deficiency of adenosine deaminase type 2 (DADA2): clinical picture, diagnosis and treatment;Vnitřní lékařství;2024-06-20

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