Varaico: Literature-Extracted Genetic Variants

Gene:UBQLN2
Variant:p.N139H
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UBQLN2

NM_013444.4:p.N139H

Associated Papers

Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2.

Vengoechea J et al.

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013

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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."