Varaico: Literature-Extracted Genetic Variants

Gene:LHX3
Variant:p.R49C
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LHX3

NM_178138.6:p.R49C

Associated Papers

Compound heterozygous and homozygous mutations of the TSHbeta gene as a cause of congenital central hypothyroidism in Europe.

Karges B et al.

Hormone Research, 2004

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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."