Cite
HARVARD Citation
Gupta, S. et al. (2017). Whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy. Medicine. 96 (30), p. . [Online].
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Gupta, S. et al. (2017). Whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy. Medicine. 96 (30), p. . [Online].