Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delay

Bosman, W., Butler, K. M., Chang, C. A., Ganapathi, M., Guzman, E., Latta, F., Chung, W. K., Claverie-Martin, F., Davis, J. M., Hoenderop, J. G. J., & de Baaij, J. H. F. (2024). Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delay. Clinical Kidney Journal, 17(8). https://doi.org/10.1093/ckj/sfae211
Authors:
Willem Bosman
Kameryn M. Butler
Chang Cj
Mythily Ganapathi
Edwin Guzman
Femke Latta
Wendy K. Chung
Félix Claveríe‐Martín
Jessica Davis
Joost G. J. Hoenderop
Jeroen H. F. de Baaij
Affiliated Authors:
Mythily Ganapathi
Edwin Guzman
Author Keywords:
autism spectrum disorder
developmental delay
genetics
hypomagnesemia
trpm7
Publication Type:
Article
Unique ID:
10.1093/ckj/sfae211
PMID:
Publication Date:
Data Source:
OpenAlex

Record Created: