Varaico: Literature-Extracted Genetic Variants

Gene:HAAO
Variant:p.W186*
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HAAO

NM_012205.3:p.W186*

Associated Papers

Nicotinamide Adenine Dinucleotide Deficiency and Its Impact on Mammalian Development.

Dunwoodie SL et al.

Antioxidants & Redox Signaling, 2023

Mitochondrial Impairment: A Common Motif in Neuropsychiatric Presentation? The Link to the Tryptophan-Kynurenine Metabolic System.

Tanaka M et al.

Cells, 2022

A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome.

Schüle I et al.

Genes, 2021

Identification of clinically actionable variants from genome sequencing of families with congenital heart disease.

Alankarage D et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019

NAD Deficiency, Congenital Malformations, and Niacin Supplementation.

Shi H et al.

The New England Journal of Medicine, 2017

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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."