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ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes - European Journal of Human Genetics

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ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes - European Journal of Human Genetics

ARHGAP35 has known roles in cell migration, invasion and division, neuronal morphogenesis, and gene/mRNA regulation; prior studies indicate a role in cancer in humans and in the developing eyes, neural tissue, and renal structures in mice.

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ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes - European Journal of Human Genetics

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ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes - European Journal of Human Genetics

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