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Structural modeling of a novel <i><scp>SLC</scp>38A8</i> mutation that causes foveal hypoplasia

25

Citations

27

References

2017

Year

Abstract

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.

References

YearCitations

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