Varaico: Literature-Extracted Genetic Variants

Gene:KCNB1
Variant:p.G321D
Back to variants list

KCNB1

NM_004975.4:p.G321D

Associated Papers

Trio-whole exome sequencing reveals the importance of de novo variants in children with intellectual disability and developmental delay.

Li C et al.

Scientific Reports, 2024

Identification of genetic causes in children with unexplained epilepsy based on trio-whole exome sequencing.

Chengyan L et al.

Clinical Genetics, 2024

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."