Varaico: Literature-Extracted Genetic Variants

Gene:TRPM7
Variant:p.M1000V
Back to variants list

TRPM7

NM_017672.6:p.M1000V

Associated Papers

Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delay.

Bosman W et al.

Clinical Kidney Journal, 2024

Case Report: Recurrent Hemiplegic Migraine Attacks Accompanied by Intractable Hypomagnesemia Due to a de novo TRPM7 Gene Variant.

Lei M et al.

Frontiers in Pediatrics, 2022

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."