Varaico: Literature-Extracted Genetic Variants

Gene:SCNN1B
Variant:p.P616_P617insFs
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SCNN1B

NM_000336.3:p.P616_P617insFs

Associated Papers

Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.

Fan P et al.

American Journal of Hypertension, 2020

32161960 (PubMed )
Supplement: hpaa037_suppl_supplementary_table_s2.doc

Liddle syndrome: clinical and genetic profiles.

Cui Y et al.

Journal of Clinical Hypertension (greenwich, Conn.), 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."