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Other gene mutations are also known to increase risk.
SDHD mutations are also subject to genomic imprinting of the maternal allele.
These mutations are also providing important new insights into nuclear cytoplasmic interactions.
Mutations are also more frequently nonsynonymous during the outbreak (Fig. 4G).
Mesp2 gene mutations are also found in human patients with spondylocostal dysostosis which is a rare, heritable axial skeleton growth disorder (Whittock et al., 2004).
With respect to viruses, interactions between mutations are also common.
Other point mutations are also found in GK1.
As both inhibitors bind to the catalytic site of NA, cross-resistance mutations are also found.
Indeed, it has been reported that OPA1 mutations are also associated with ptosis and ophthalmoplegia [27], [28], [29].
It will be of interest to determine if LKB1 mutations are also useful prognostically in other cancers [9].
In this study we demonstrated that PD patients with LRRK2 mutations are also different from the control subjects.
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