Varaico: Literature-Extracted Genetic Variants

Gene:INS
Variant:p.T97delFs
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INS

NM_000207.3:p.T97delFs

Associated Papers

A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC).

Wevers RA et al.

Journal of Inherited Metabolic Disease, 1999

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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."