Varaico: Literature-Extracted Genetic Variants

Gene:ASMT
Variant:p.L326F
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ASMT

NM_001171038.2:p.L326F

Associated Papers

Biogenic Amine Metabolism and Its Genetic Variations in Autism Spectrum Disorder: A Comprehensive Overview.

Tabolacci C et al.

Biomolecules, 2025

Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway.

Botros HG et al.

Journal of Pineal Research, 2013

Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder.

Etain B et al.

Human Molecular Genetics, 2012

Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.

Chaste P et al.

Journal of Pineal Research, 2011

Abnormal melatonin synthesis in autism spectrum disorders.

Melke J et al.

Molecular Psychiatry, 2008

Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations.

Toma C et al.

Molecular Psychiatry, 2007

The possible interplay of synaptic and clock genes in autism spectrum disorders.

Bourgeron T

Cold Spring Harbor Symposia on Quantitative Biology, 2007

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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."