Article info

Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

Authors

  1. Correspondence to Dr Christina Torres Kozycki; christina.kozycki{at}nih.gov; Dr Daniel L Kastner; dan.kastner{at}nih.gov
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Citation

Kozycki CT, Kodati S, Huryn L Undiagnosed Diseases Network, et al
Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

Publication history

  • Received April 8, 2022
  • Accepted June 6, 2022
  • First published July 22, 2022.
Online issue publication 
September 12, 2022

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  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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