Varaico: Literature-Extracted Genetic Variants

Gene:FMNL3
Variant:p.F38L
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FMNL3

NM_175736.5:p.F38L

Associated Papers

Formins in Human Disease.

Labat-de-Hoz L et al.

Cells, 2021

Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.

Kumar R et al.

Human Molecular Genetics, 2015

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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."