Cite
HARVARD Citation
Feng, L. et al. (2017). Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family. Medicine. 96 (24), p. . [Online].
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Feng, L. et al. (2017). Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family. Medicine. 96 (24), p. . [Online].