Varaico: Literature-Extracted Genetic Variants

Gene:SLC5A6
Variant:p.Q622delFs
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SLC5A6

NM_021095.4:p.Q622delFs

Associated Papers

Expanded Clinical Phenotype and the Role of Untargeted Metabolomics Analysis in Confirming the Diagnosis of Sodium-Dependent Multivitamin Transporter Deficiency.

Walimbe AS et al.

American Journal of Medical Genetics. Part A, 2025

SLC5A6 Mutations in Axonal Sensorimotor Polyneuropathy Patients Concurrent With Sodium Dependent Multivitamin Transporter Deficiency and Improved Effects by Multivitamin Therapy.

Pi BK et al.

Journal of the Peripheral Nervous System : Jpns, 2025

A novel SLC5A6 homozygous variant in a family with multivitamin-dependent neurometabolic disorder: Phenotype expansion and long-term follow-up.

Montomoli M et al.

European Journal of Medical Genetics, 2023

Sodium-dependent multivitamin transporter defects: a rare cause of recurrent vomiting and faltering growth.

Rupasinghe K et al.

Frontline Gastroenterology, 2023

A mild case of sodium-dependent multivitamin transporter (SMVT) deficiency illustrating the importance of treatment response in variant classification.

Hauth I et al.

Cold Spring Harbor Molecular Case Studies, 2022

Genetic defect of the sodium-dependent multivitamin transporter: A treatable disease, mimicking biotinidase deficiency.

Schwantje M et al.

Jimd Reports, 2019

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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."