Varaico: Literature-Extracted Genetic Variants

Gene:MYH2
Variant:p.F801fs
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MYH2

NM_017534.6:p.F801fs

Associated Papers

A novel MYH2 mutation in family members presenting with congenital myopathy, ophthalmoplegia and facial weakness.

Willis T et al.

Journal of Neurology, 2016

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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."