Undetectable C1Q, hyper-IgM, hypogammaglobulinemia: whole exome sequencing reveals pathogenic variant in magnesium transporter 1 (MAGT1)

Authors

S. L. Leo, LSU Health Sciences Center - New Orleans
J. Upadia, Tulane University, New Orleans, LA
S. Valley, Children's Hospital, New Orleans, LA
Luke A. Wall, LSU Health Sciences Center - New OrleansFollow

Document Type

Conference Proceeding

Publication Date

2-1-2024

Publication Title

American Journal of the Medical Sciences

Abstract

The American Journal of the Medical Sciences Annual Meeting; Feb 22 - Feb 24, 2024; New Orleans, LA

First Page

S327

Last Page

S328

Volume

367

Comments

Abstract 5476

Recommended Citation

Leo, S. L.; Upadia, J.; Valley, S.; and Wall, Luke A., "Undetectable C1Q, hyper-IgM, hypogammaglobulinemia: whole exome sequencing reveals pathogenic variant in magnesium transporter 1 (MAGT1)" (2024). School of Medicine Faculty Publications. 3141.
https://digitalscholar.lsuhsc.edu/som_facpubs/3141
10.1016/S0002-9629(24)00598-6