Publication | Open Access
Structural modeling of a novel <i><scp>SLC</scp>38A8</i> mutation that causes foveal hypoplasia
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Citations
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References
2017
Year
Our results demonstrate a novel use for OCT-angiography in confirming FH, and also uncover genotype-phenotype correlations of FH-linked <i>SLC38A8</i> mutations.
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